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| Open reading frame (ORF) annotation in the exon skipping event |
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| Splicing Quantitative Trait Loci (sQTLs) in the skipped exons |
| Splicing Quantitative Trait Methylation (sQTM) in the skipped exon |
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Gene summary for TP53 |
 Gene summary |
| Gene information | Gene symbol | TP53 | Gene ID | 7157 |
| Gene name | tumor protein p53 | |
| Synonyms | BCC7|LFS1|P53|TRP53 | |
| Cytomap | 17p13.1 | |
| Type of gene | protein-coding | |
| Description | cellular tumor antigen p53antigen NY-CO-13mutant tumor protein 53p53 tumor suppressorphosphoprotein p53transformation-related protein 53tumor protein 53tumor supressor p53 | |
| Modification date | 20180527 | |
| UniProtAcc | P04637 | |
| Context | PubMed: TP53 [Title/Abstract] AND exon [Title/Abstract] AND skip [Title/Abstract] - Title (PMID) |
| Gene ontology of each this gene with evidence of Inferred from Direct Assay (IDA) from Entrez |
| Gene | GO ID | GO term | PubMed ID |
| TP53 | GO:0000733 | DNA strand renaturation | 8183576 |
| TP53 | GO:0006355 | regulation of transcription, DNA-templated | 7587074 |
| TP53 | GO:0006974 | cellular response to DNA damage stimulus | 14744935|15710329|17938203 |
| TP53 | GO:0006978 | DNA damage response, signal transduction by p53 class mediator resulting in transcription of p21 class mediator | 16213212 |
| TP53 | GO:0006983 | ER overload response | 14744935 |
| TP53 | GO:0007050 | cell cycle arrest | 15149599 |
| TP53 | GO:0008104 | protein localization | 16507995 |
| TP53 | GO:0008285 | negative regulation of cell proliferation | 22783376 |
| TP53 | GO:0010628 | positive regulation of gene expression | 15314173|20332243 |
| TP53 | GO:0030330 | DNA damage response, signal transduction by p53 class mediator | 15149599 |
| TP53 | GO:0031497 | chromatin assembly | 16322561 |
| TP53 | GO:0032461 | positive regulation of protein oligomerization | 12667443 |
| TP53 | GO:0034644 | cellular response to UV | 16213212|23629966 |
| TP53 | GO:0042149 | cellular response to glucose starvation | 14744935|21471221 |
| TP53 | GO:0042771 | intrinsic apoptotic signaling pathway in response to DNA damage by p53 class mediator | 14654789|14744935|17403783 |
| TP53 | GO:0042981 | regulation of apoptotic process | 14744935 |
| TP53 | GO:0043065 | positive regulation of apoptotic process | 12667443|15565177|20959462 |
| TP53 | GO:0045892 | negative regulation of transcription, DNA-templated | 24051492 |
| TP53 | GO:0045893 | positive regulation of transcription, DNA-templated | 16322561|17403783|18549481|20378837 |
| TP53 | GO:0045899 | positive regulation of RNA polymerase II transcriptional preinitiation complex assembly | 24289924 |
| TP53 | GO:0045944 | positive regulation of transcription by RNA polymerase II | 11672523|17310983|17599062|18549481|20959462|24652652 |
| TP53 | GO:0051974 | negative regulation of telomerase activity | 10597287 |
| TP53 | GO:0065003 | protein-containing complex assembly | 12915590 |
| TP53 | GO:0071158 | positive regulation of cell cycle arrest | 15314173 |
| TP53 | GO:0071480 | cellular response to gamma radiation | 16213212 |
| TP53 | GO:0072331 | signal transduction by p53 class mediator | 15314173 |
| TP53 | GO:0072717 | cellular response to actinomycin D | 15314173 |
| TP53 | GO:0090200 | positive regulation of release of cytochrome c from mitochondria | 12667443|14963330 |
| TP53 | GO:0097252 | oligodendrocyte apoptotic process | 7720704 |
| TP53 | GO:1902895 | positive regulation of pri-miRNA transcription by RNA polymerase II | 20546595 |
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Exon skipping events across known transcript of Ensembl for TP53 from UCSC genome browser |
| Skipped exons in TCGA and GTEx based on Ensembl gene isoform structure. * Click on the image to open the UCSC genome browser with custom track showing this image in a new window. |
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Gene isoform structures and expression levels for TP53 |
| Expression levels of gene isoforms across TCGA. |
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| Expression levels of gene isoforms across GTEx. |
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Exon skipping events with PSIs in TCGA for TP53 |
| Information of exkip skipping event in TCGA. |
| Exon skip ID | chr | Exons involved in exon skipping | Skipped exon | ENSG | ENSTs |
| exon_skip_286364 | 17 | 7572886:7573008:7573926:7574033:7576852:7576905 | 7573926:7574033 | ENSG00000141510.11 | ENST00000445888.2,ENST00000269305.4,ENST00000504937.1 |
| exon_skip_286366 | 17 | 7573926:7574033:7576524:7576584:7576852:7576926 | 7576524:7576584 | ENSG00000141510.11 | ENST00000455263.2,ENST00000504290.1 |
| exon_skip_286367 | 17 | 7573926:7574033:7576524:7576657:7576852:7576905 | 7576524:7576657 | ENSG00000141510.11 | ENST00000510385.1,ENST00000420246.2 |
| exon_skip_286371 | 17 | 7573926:7574033:7576852:7576926:7577018:7577155 | 7576852:7576926 | ENSG00000141510.11 | ENST00000445888.2,ENST00000269305.4,ENST00000504937.1 |
| exon_skip_286376 | 17 | 7576852:7576926:7577018:7577155:7577498:7577608 | 7577018:7577155 | ENSG00000141510.11 | ENST00000455263.2,ENST00000510385.1,ENST00000509690.1,ENST00000420246.2,ENST00000445888.2,ENST00000504290.1,ENST00000359597.4,ENST00000269305.4,ENST00000504937.1 |
| exon_skip_286379 | 17 | 7577571:7577608:7578176:7578289:7578370:7578437 | 7578176:7578289 | ENSG00000141510.11 | ENST00000455263.2,ENST00000510385.1,ENST00000509690.1,ENST00000514944.1,ENST00000413465.2,ENST00000420246.2,ENST00000445888.2,ENST00000504290.1,ENST00000359597.4,ENST00000269305.4,ENST00000504937.1 |
| exon_skip_286384 | 17 | 7578546:7578554:7579311:7579590:7579699:7579721 | 7579311:7579590 | ENSG00000141510.11 | ENST00000455263.2,ENST00000505014.1,ENST00000413465.2,ENST00000503591.1,ENST00000508793.1,ENST00000420246.2,ENST00000445888.2,ENST00000359597.4,ENST00000269305.4 |
| exon_skip_286388 | 17 | 7579311:7579590:7579699:7579721:7579838:7579912 | 7579699:7579721 | ENSG00000141510.11 | ENST00000455263.2,ENST00000503591.1,ENST00000508793.1,ENST00000420246.2,ENST00000445888.2,ENST00000359597.4,ENST00000269305.4,ENST00000604348.1 |
| exon_skip_286389 | 17 | 7579838:7579940:7580642:7580745:7590694:7590745 | 7580642:7580745 | ENSG00000141510.11 | ENST00000503591.1 |
| PSI values of skipped exons in TCGA. |
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Exon skipping events with PSIs in GTEx for TP53 |
| Information of exkip skipping event in GTEx |
| Exon skip ID | chr | Exons involved in exon skipping | Skipped exon | ENSG | ENSTs |
| exon_skip_286364 | 17 | 7572886:7573008:7573926:7574033:7576852:7576905 | 7573926:7574033 | ENSG00000141510.11 | ENST00000504937.1,ENST00000269305.4,ENST00000445888.2 |
| exon_skip_286366 | 17 | 7573926:7574033:7576524:7576584:7576852:7576926 | 7576524:7576584 | ENSG00000141510.11 | ENST00000504290.1,ENST00000455263.2 |
| exon_skip_286367 | 17 | 7573926:7574033:7576524:7576657:7576852:7576905 | 7576524:7576657 | ENSG00000141510.11 | ENST00000510385.1,ENST00000420246.2 |
| exon_skip_286379 | 17 | 7577571:7577608:7578176:7578289:7578370:7578437 | 7578176:7578289 | ENSG00000141510.11 | ENST00000413465.2,ENST00000359597.4,ENST00000504290.1,ENST00000510385.1,ENST00000504937.1,ENST00000269305.4,ENST00000455263.2,ENST00000420246.2,ENST00000445888.2,ENST00000509690.1,ENST00000514944.1 |
| exon_skip_286384 | 17 | 7578546:7578554:7579311:7579590:7579699:7579721 | 7579311:7579590 | ENSG00000141510.11 | ENST00000413465.2,ENST00000359597.4,ENST00000269305.4,ENST00000455263.2,ENST00000420246.2,ENST00000445888.2,ENST00000505014.1,ENST00000508793.1,ENST00000503591.1 |
| exon_skip_286389 | 17 | 7579838:7579940:7580642:7580745:7590694:7590745 | 7580642:7580745 | ENSG00000141510.11 | ENST00000503591.1 |
| PSI values of skipped exons in GTEx. |
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| * Skipped exon sequences. |
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Open reading frame (ORF) annotation in the exon skipping event for TP53 |
| Open reading frame (ORF) of individual exon skipping events in TCGA based on the Ensembl gene structure combined from isoforms. |
| ENST | Start of skipped exon | End of skipped exon | ORF |
| ENST00000269305 | 7573926 | 7574033 | Frame-shift |
| ENST00000445888 | 7573926 | 7574033 | Frame-shift |
| ENST00000269305 | 7576852 | 7576926 | Frame-shift |
| ENST00000445888 | 7576852 | 7576926 | Frame-shift |
| ENST00000269305 | 7577018 | 7577155 | Frame-shift |
| ENST00000445888 | 7577018 | 7577155 | Frame-shift |
| ENST00000269305 | 7578176 | 7578289 | Frame-shift |
| ENST00000445888 | 7578176 | 7578289 | Frame-shift |
| ENST00000269305 | 7579699 | 7579721 | Frame-shift |
| ENST00000445888 | 7579699 | 7579721 | Frame-shift |
| ENST00000269305 | 7579311 | 7579590 | In-frame |
| ENST00000445888 | 7579311 | 7579590 | In-frame |
| Open reading frame (ORF) of individual exon skipping events in GTEx based on the Ensembl gene structure combined from isoforms. |
| ENST | Start of skipped exon | End of skipped exon | ORF |
| ENST00000269305 | 7573926 | 7574033 | Frame-shift |
| ENST00000445888 | 7573926 | 7574033 | Frame-shift |
| ENST00000269305 | 7578176 | 7578289 | Frame-shift |
| ENST00000445888 | 7578176 | 7578289 | Frame-shift |
| ENST00000269305 | 7579311 | 7579590 | In-frame |
| ENST00000445888 | 7579311 | 7579590 | In-frame |
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Infer the effects of exon skipping event on protein functional features for TP53 |
| Exon skipping at the protein sequence level and followed lost functional features. * Click on the image to enlarge it in a new window. |
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| Loci of skipped exons in TCGA across genomic, transcript, and protein sequence levels of In-frame cases. |
| ENST | Length of mRNA | Length of AA seq. | Genomic start | Genomic end | mRNA start | mRNA end | AA start | AA end |
| ENST00000269305 | 2596 | 393 | 7579311 | 7579590 | 287 | 565 | 32 | 125 |
| ENST00000445888 | 2523 | 393 | 7579311 | 7579590 | 233 | 511 | 32 | 125 |
| Loci of skipped exons in GTEx across genomic, transcript, and protein sequence levels of In-frame cases. |
| ENST | Length of mRNA | Length of AA seq. | Genomic start | Genomic end | mRNA start | mRNA end | AA start | AA end |
| ENST00000269305 | 2596 | 393 | 7579311 | 7579590 | 287 | 565 | 32 | 125 |
| ENST00000445888 | 2523 | 393 | 7579311 | 7579590 | 233 | 511 | 32 | 125 |
| Lost protein functional features of individual exon skipping events in TCGA. |
| UniProt acc. | Start of exon skipping (AA) | End of exon skipping (AA) | Protein feature start (AA) | Protein feature end (AA) | Category of protein feature | Description of feature |
| Lost protein functional features of individual exon skipping events in GTEx. |
| UniProt acc. | Start of exon skipping (AA) | End of exon skipping (AA) | Protein feature start (AA) | Protein feature end (AA) | Category of protein feature | Description of feature |
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SNVs in the skipped exons for TP53 |
| - Lollipop plot for presenting exon skipping associated SNVs. * Click on the image to enlarge it in a new window. |
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| - Differential PSIs between mutated versus non-mutated samples. |
TP53_BRCA_exon_skip_286364_psi_boxplot.png |
TP53_BRCA_exon_skip_286371_psi_boxplot.png |
TP53_BRCA_exon_skip_286376_psi_boxplot.png |
TP53_BRCA_exon_skip_286379_psi_boxplot.png |
TP53_BRCA_exon_skip_286384_psi_boxplot.png |
TP53_COAD_exon_skip_286364_psi_boxplot.png |
TP53_COAD_exon_skip_286371_psi_boxplot.png |
TP53_COAD_exon_skip_286376_psi_boxplot.png |
TP53_COAD_exon_skip_286379_psi_boxplot.png |
TP53_COAD_exon_skip_286384_psi_boxplot.png |
TP53_DLBC_exon_skip_286364_psi_boxplot.png |
TP53_ESCA_exon_skip_286364_psi_boxplot.png |
TP53_ESCA_exon_skip_286371_psi_boxplot.png |
TP53_ESCA_exon_skip_286376_psi_boxplot.png |
TP53_ESCA_exon_skip_286379_psi_boxplot.png |
TP53_ESCA_exon_skip_286384_psi_boxplot.png |
TP53_GBM_exon_skip_286379_psi_boxplot.png |
TP53_HNSC_exon_skip_286371_psi_boxplot.png |
TP53_HNSC_exon_skip_286376_psi_boxplot.png |
TP53_HNSC_exon_skip_286379_psi_boxplot.png |
TP53_HNSC_exon_skip_286384_psi_boxplot.png |
TP53_HNSC_exon_skip_286388_psi_boxplot.png |
TP53_KICH_exon_skip_286388_psi_boxplot.png |
TP53_KIRC_exon_skip_286379_psi_boxplot.png |
TP53_KIRP_exon_skip_286384_psi_boxplot.png |
TP53_LGG_exon_skip_286364_psi_boxplot.png |
TP53_LGG_exon_skip_286376_psi_boxplot.png |
TP53_LGG_exon_skip_286379_psi_boxplot.png |
TP53_LGG_exon_skip_286384_psi_boxplot.png |
TP53_LGG_exon_skip_286388_psi_boxplot.png |
TP53_LIHC_exon_skip_286371_psi_boxplot.png |
TP53_LIHC_exon_skip_286376_psi_boxplot.png |
TP53_LIHC_exon_skip_286384_psi_boxplot.png |
TP53_LUAD_exon_skip_286364_psi_boxplot.png |
TP53_LUAD_exon_skip_286371_psi_boxplot.png |
TP53_LUAD_exon_skip_286376_psi_boxplot.png |
TP53_LUAD_exon_skip_286379_psi_boxplot.png |
TP53_LUAD_exon_skip_286384_psi_boxplot.png |
TP53_LUSC_exon_skip_286364_psi_boxplot.png |
TP53_LUSC_exon_skip_286371_psi_boxplot.png |
TP53_LUSC_exon_skip_286376_psi_boxplot.png |
TP53_LUSC_exon_skip_286379_psi_boxplot.png |
TP53_LUSC_exon_skip_286384_psi_boxplot.png |
TP53_OV_exon_skip_286364_psi_boxplot.png |
TP53_OV_exon_skip_286371_psi_boxplot.png |
TP53_OV_exon_skip_286376_psi_boxplot.png |
TP53_OV_exon_skip_286379_psi_boxplot.png |
TP53_OV_exon_skip_286384_psi_boxplot.png |
TP53_PAAD_exon_skip_286371_psi_boxplot.png |
TP53_PAAD_exon_skip_286376_psi_boxplot.png |
TP53_PAAD_exon_skip_286379_psi_boxplot.png |
TP53_PAAD_exon_skip_286384_psi_boxplot.png |
TP53_PRAD_exon_skip_286379_psi_boxplot.png |
TP53_PRAD_exon_skip_286384_psi_boxplot.png |
TP53_READ_exon_skip_286379_psi_boxplot.png |
TP53_READ_exon_skip_286384_psi_boxplot.png |
TP53_SARC_exon_skip_286364_psi_boxplot.png |
TP53_SARC_exon_skip_286376_psi_boxplot.png |
TP53_SARC_exon_skip_286384_psi_boxplot.png |
TP53_SKCM_exon_skip_286364_psi_boxplot.png |
TP53_SKCM_exon_skip_286371_psi_boxplot.png |
TP53_SKCM_exon_skip_286379_psi_boxplot.png |
TP53_SKCM_exon_skip_286384_psi_boxplot.png |
TP53_STAD_exon_skip_286364_psi_boxplot.png |
TP53_STAD_exon_skip_286376_psi_boxplot.png |
TP53_STAD_exon_skip_286379_psi_boxplot.png |
TP53_STAD_exon_skip_286384_psi_boxplot.png |
TP53_UCEC_exon_skip_286371_psi_boxplot.png |
TP53_UCS_exon_skip_286379_psi_boxplot.png |
TP53_UCS_exon_skip_286384_psi_boxplot.png |
| - Non-synonymous mutations located in the skipped exons in TCGA. |
| Cancer type | Sample | ESID | Skipped exon start | Skipped exon end | Mutation start | Mutation end | Mutation type | Reference seq | Mutation seq | AAchange |
| OV | TCGA-24-1434-01 | exon_skip_286364 | 7573927 | 7574033 | 7573995 | 7573995 | Frame_Shift_Del | C | - | p.L344fs |
| LGG | TCGA-HT-7873-01 | exon_skip_286364 | 7573927 | 7574033 | 7573996 | 7574003 | Frame_Shift_Del | AGCTCTCG | - | p.303_305del |
| LGG | TCGA-HT-7873-01 | exon_skip_286364 | 7573927 | 7574033 | 7573996 | 7574003 | Frame_Shift_Del | AGCTCTCG | - | p.REL342fs |
| THCA | TCGA-EL-A3D5-01 | exon_skip_286364 | 7573927 | 7574033 | 7573998 | 7573999 | Frame_Shift_Del | CT | - | p.304_305del |
| THCA | TCGA-EL-A3D5-01 | exon_skip_286364 | 7573927 | 7574033 | 7573998 | 7573999 | Frame_Shift_Del | CT | - | p.E343fs |
| BRCA | TCGA-AR-A1AQ-01 | exon_skip_286364 | 7573927 | 7574033 | 7574003 | 7574003 | Frame_Shift_Del | G | - | p.R342fs |
| HNSC | TCGA-CR-6477-01 | exon_skip_286364 | 7573927 | 7574033 | 7574003 | 7574003 | Frame_Shift_Del | G | - | p.R342fs |
| PAAD | TCGA-HV-A5A6-01 | exon_skip_286364 | 7573927 | 7574033 | 7574003 | 7574003 | Frame_Shift_Del | G | - | p.R342fs |
| STAD | TCGA-VQ-A91U-01 | exon_skip_286364 | 7573927 | 7574033 | 7574003 | 7574003 | Frame_Shift_Del | G | - | p.R342fs |
| LUAD | TCGA-55-6712-01 | exon_skip_286364 | 7573927 | 7574033 | 7574012 | 7574012 | Frame_Shift_Del | C | - | p.E339fs |
| STAD | TCGA-CD-A4MH-01 | exon_skip_286364 | 7573927 | 7574033 | 7574012 | 7574012 | Frame_Shift_Del | C | - | p.E339fs |
| SARC | TCGA-IE-A4EI-01 | exon_skip_286364 | 7573927 | 7574033 | 7574019 | 7574020 | Frame_Shift_Del | CT | - | p.E336fs |
| ACC | TCGA-OR-A5JL-01 | exon_skip_286364 | 7573927 | 7574033 | 7574023 | 7574023 | Frame_Shift_Del | C | - | p.R296fs |
| ACC | TCGA-OR-A5JL-01 | exon_skip_286364 | 7573927 | 7574033 | 7574023 | 7574023 | Frame_Shift_Del | C | - | p.R335fs |
| LGG | TCGA-DH-5140-01 | exon_skip_286364 | 7573927 | 7574033 | 7574025 | 7574025 | Frame_Shift_Del | C | - | p.G334fs |
| LGG | TCGA-DH-5140-01 | exon_skip_286364 | 7573927 | 7574033 | 7574025 | 7574025 | Frame_Shift_Del | C | - | p.R296fs |
| SARC | TCGA-WK-A8Y0-01 | exon_skip_286364 | 7573927 | 7574033 | 7574025 | 7574025 | Frame_Shift_Del | C | - | p.G334fs |
| SARC | TCGA-WK-A8Y0-01 | exon_skip_286364 | 7573927 | 7574033 | 7574025 | 7574025 | Frame_Shift_Del | C | - | p.R335fs |
| BRCA | TCGA-A2-A0YM-01 | exon_skip_286364 | 7573927 | 7574033 | 7574030 | 7574030 | Frame_Shift_Del | G | - | p.R333fs |
| LUAD | TCGA-97-A4M0-01 | exon_skip_286364 | 7573927 | 7574033 | 7574030 | 7574030 | Frame_Shift_Del | G | - | p.R333fs |
| OV | TCGA-13-1497-01 | exon_skip_286364 | 7573927 | 7574033 | 7574030 | 7574030 | Frame_Shift_Del | G | - | p.R333fs |
| LIHC | TCGA-DD-AACM-01 | exon_skip_286371 | 7576853 | 7576926 | 7576854 | 7576860 | Frame_Shift_Del | TGAAGGG | - | p.329_331del |
| HNSC | TCGA-CN-6995-01 | exon_skip_286371 | 7576853 | 7576926 | 7576858 | 7576858 | Frame_Shift_Del | G | - | p.L330fs |
| OV | TCGA-13-1509-01 | exon_skip_286371 | 7576853 | 7576926 | 7576858 | 7576858 | Frame_Shift_Del | G | - | p.L330fs |
| BRCA | TCGA-A8-A07U-01 | exon_skip_286371 | 7576853 | 7576926 | 7576863 | 7576863 | Frame_Shift_Del | A | - | p.F328fs |
| LIHC | TCGA-DD-AACE-01 | exon_skip_286371 | 7576853 | 7576926 | 7576863 | 7576863 | Frame_Shift_Del | A | - | p.F328fs |
| LIHC | TCGA-CC-A7IK-01 | exon_skip_286371 | 7576853 | 7576926 | 7576866 | 7576866 | Frame_Shift_Del | T | - | p.Y327fs |
| LIHC | TCGA-CC-A7IK-01 | exon_skip_286371 | 7576853 | 7576926 | 7576866 | 7576897 | Frame_Shift_Del | TATTCTCCATCCAGTGGTTTCTTCTTTGGCTG | - | p.317_327del |
| HNSC | TCGA-DQ-5630-01 | exon_skip_286371 | 7576853 | 7576926 | 7576868 | 7576886 | Frame_Shift_Del | TTCTCCATCCAGTGGTTTC | - | p.K320fs |
| HNSC | TCGA-DQ-5630-01 | exon_skip_286371 | 7576853 | 7576926 | 7576868 | 7576886 | Frame_Shift_Del | TTCTCCATCCAGTGGTTTC | - | p.KKPLDGE320fs |
| LUSC | TCGA-63-5128-01 | exon_skip_286371 | 7576853 | 7576926 | 7576878 | 7576887 | Frame_Shift_Del | AGTGGTTTCT | - | p.K320fs |
| BRCA | TCGA-A2-A0D2-01 | exon_skip_286371 | 7576853 | 7576926 | 7576885 | 7576895 | Frame_Shift_Del | TCTTCTTTGGC | - | p.P318fs |
| PRAD | TCGA-EJ-7781-01 | exon_skip_286371 | 7576853 | 7576926 | 7576890 | 7576890 | Frame_Shift_Del | T | - | p.K319fs |
| PRAD | TCGA-EJ-7781-01 | exon_skip_286371 | 7576853 | 7576926 | 7576890 | 7576890 | Frame_Shift_Del | T | - | p.K321fs |
| LUSC | TCGA-43-3394-01 | exon_skip_286371 | 7576853 | 7576926 | 7576904 | 7576904 | Frame_Shift_Del | G | - | p.S314fs |
| GBM | TCGA-06-0128-01 | exon_skip_286371 | 7576853 | 7576926 | 7576910 | 7576910 | Frame_Shift_Del | G | - | p.T312fs |
| LUAD | TCGA-55-6968-01 | exon_skip_286371 | 7576853 | 7576926 | 7576910 | 7576910 | Frame_Shift_Del | G | - | p.T312fs |
| STAD | TCGA-RD-A8N9-01 | exon_skip_286371 | 7576853 | 7576926 | 7576919 | 7576919 | Frame_Shift_Del | G | - | p.N310fs |
| STAD | TCGA-RD-A8N9-01 | exon_skip_286371 | 7576853 | 7576926 | 7576919 | 7576919 | Frame_Shift_Del | G | - | p.P309fs |
| ESCA | TCGA-L5-A4OJ-01 | exon_skip_286371 | 7576853 | 7576926 | 7576921 | 7576925 | Frame_Shift_Del | GCAGT | - | p.308_309del |
| BRCA | TCGA-C8-A138-01 | exon_skip_286371 | 7576853 | 7576926 | 7576924 | 7576925 | Frame_Shift_Del | GT | - | p.L308fs |
| LUAD | TCGA-55-6975-01 | exon_skip_286376 | 7577019 | 7577155 | 7577022 | 7577025 | Frame_Shift_Del | GCTT | - | p.KR305fs |
| LIHC | TCGA-DD-AAE8-01 | exon_skip_286376 | 7577019 | 7577155 | 7577023 | 7577033 | Frame_Shift_Del | CTTAGTGCTCC | - | p.302_306del |
| SARC | TCGA-K1-A42W-01 | exon_skip_286376 | 7577019 | 7577155 | 7577029 | 7577032 | Frame_Shift_Del | GCTC | - | p.GS302fs |
| SARC | TCGA-K1-A42W-01 | exon_skip_286376 | 7577019 | 7577155 | 7577029 | 7577032 | Frame_Shift_Del | GCTC | - | p.S303fs |
| BRCA | TCGA-B6-A0RE-01 | exon_skip_286376 | 7577019 | 7577155 | 7577031 | 7577031 | Frame_Shift_Del | T | - | p.S303fs |
| HNSC | TCGA-CV-6948-01 | exon_skip_286376 | 7577019 | 7577155 | 7577032 | 7577033 | Frame_Shift_Del | CC | - | p.G302fs |
| BLCA | TCGA-E7-A97Q-01 | exon_skip_286376 | 7577019 | 7577155 | 7577036 | 7577036 | Frame_Shift_Del | G | - | p.P301fs |
| COAD | TCGA-AA-3492-01 | exon_skip_286376 | 7577019 | 7577155 | 7577036 | 7577036 | Frame_Shift_Del | G | - | p.P301fs |
| STAD | TCGA-BR-4363-01 | exon_skip_286376 | 7577019 | 7577155 | 7577036 | 7577036 | Frame_Shift_Del | G | - | p.P301fs |
| STAD | TCGA-BR-8081-01 | exon_skip_286376 | 7577019 | 7577155 | 7577036 | 7577036 | Frame_Shift_Del | G | - | p.P301fs |
| HNSC | TCGA-CN-A498-01 | exon_skip_286376 | 7577019 | 7577155 | 7577048 | 7577048 | Frame_Shift_Del | T | - | p.H297fs |
| LGG | TCGA-S9-A89Z-01 | exon_skip_286376 | 7577019 | 7577155 | 7577049 | 7577049 | Frame_Shift_Del | G | - | p.H297fs |
| BRCA | TCGA-A2-A0T3-01 | exon_skip_286376 | 7577019 | 7577155 | 7577051 | 7577079 | Frame_Shift_Del | TGAGGCTCCCCTTTCTTGCGGAGATTCTC | - | p.E287fs |
| LUAD | TCGA-55-8511-01 | exon_skip_286376 | 7577019 | 7577155 | 7577052 | 7577052 | Frame_Shift_Del | G | - | p.H297fs |
| LUAD | TCGA-55-7914-01 | exon_skip_286376 | 7577019 | 7577155 | 7577058 | 7577058 | Frame_Shift_Del | C | - | p.E294fs |
| BRCA | TCGA-EW-A1PH-01 | exon_skip_286376 | 7577019 | 7577155 | 7577061 | 7577064 | Frame_Shift_Del | CTTT | - | p.K292fs |
| ESCA | TCGA-XP-A8T7-01 | exon_skip_286376 | 7577019 | 7577155 | 7577062 | 7577062 | Frame_Shift_Del | T | - | p.E294fs |
| ESCA | TCGA-XP-A8T7-01 | exon_skip_286376 | 7577019 | 7577155 | 7577062 | 7577062 | Frame_Shift_Del | T | - | p.G293fs |
| ESCA | TCGA-XP-A8T7-01 | exon_skip_286376 | 7577019 | 7577155 | 7577062 | 7577062 | Frame_Shift_Del | T | - | p.K292fs |
| HNSC | TCGA-CX-7086-01 | exon_skip_286376 | 7577019 | 7577155 | 7577062 | 7577062 | Frame_Shift_Del | T | - | p.K292fs |
| BLCA | TCGA-K4-A54R-01 | exon_skip_286376 | 7577019 | 7577155 | 7577065 | 7577065 | Frame_Shift_Del | C | - | p.K292fs |
| BRCA | TCGA-BH-A18U-01 | exon_skip_286376 | 7577019 | 7577155 | 7577067 | 7577085 | Frame_Shift_Del | TGCGGAGATTCTCTTCCTC | - | p.E285fs |
| LGG | TCGA-DU-6399-01 | exon_skip_286376 | 7577019 | 7577155 | 7577081 | 7577099 | Frame_Shift_Del | TCCTCTGTGCGCCGGTCTC | - | p.148_154del |
| LGG | TCGA-DU-6399-01 | exon_skip_286376 | 7577019 | 7577155 | 7577081 | 7577099 | Frame_Shift_Del | TCCTCTGTGCGCCGGTCTC | - | p.RDRRTEE280fs |
| STAD | TCGA-D7-6822-01 | exon_skip_286376 | 7577019 | 7577155 | 7577087 | 7577087 | Frame_Shift_Del | G | - | p.T284fs |
| OV | TCGA-24-2267-01 | exon_skip_286376 | 7577019 | 7577155 | 7577088 | 7577088 | Frame_Shift_Del | T | - | p.T284fs |
| STAD | TCGA-D7-6818-01 | exon_skip_286376 | 7577019 | 7577155 | 7577090 | 7577096 | Frame_Shift_Del | CGCCGGT | - | p.281_283del |
| STAD | TCGA-D7-6818-01 | exon_skip_286376 | 7577019 | 7577155 | 7577090 | 7577096 | Frame_Shift_Del | CGCCGGT | - | p.D281fs |
| HNSC | TCGA-CN-5363-01 | exon_skip_286376 | 7577019 | 7577155 | 7577092 | 7577092 | Frame_Shift_Del | C | - | p.R282fs |
| HNSC | TCGA-CN-5363-01 | exon_skip_286376 | 7577019 | 7577155 | 7577092 | 7577092 | Frame_Shift_Del | C | - | p.R283fs |
| SARC | TCGA-X9-A971-01 | exon_skip_286376 | 7577019 | 7577155 | 7577093 | 7577094 | Frame_Shift_Del | CG | - | p.R283fs |
| GBM | TCGA-27-2519-01 | exon_skip_286376 | 7577019 | 7577155 | 7577094 | 7577094 | Frame_Shift_Del | G | - | p.R282fs |
| THYM | TCGA-3S-A8YW-01 | exon_skip_286376 | 7577019 | 7577155 | 7577096 | 7577096 | Frame_Shift_Del | T | - | p.D281fs |
| LGG | TCGA-E1-5302-01 | exon_skip_286376 | 7577019 | 7577155 | 7577101 | 7577101 | Frame_Shift_Del | C | - | p.G279fs |
| LGG | TCGA-E1-5302-01 | exon_skip_286376 | 7577019 | 7577155 | 7577101 | 7577101 | Frame_Shift_Del | C | - | p.R148fs |
| LGG | TCGA-CS-6665-01 | exon_skip_286376 | 7577019 | 7577155 | 7577105 | 7577105 | Frame_Shift_Del | G | - | p.P146fs |
| LGG | TCGA-CS-6665-01 | exon_skip_286376 | 7577019 | 7577155 | 7577105 | 7577105 | Frame_Shift_Del | G | - | p.P278fs |
| LGG | TCGA-S9-A7R7-01 | exon_skip_286376 | 7577019 | 7577155 | 7577105 | 7577105 | Frame_Shift_Del | G | - | p.P278fs |
| BRCA | TCGA-AN-A0XU-01 | exon_skip_286376 | 7577019 | 7577155 | 7577107 | 7577116 | Frame_Shift_Del | ACAGGCACAA | - | p.C275fs |
| SKCM | TCGA-FS-A4F9-06 | exon_skip_286376 | 7577019 | 7577155 | 7577112 | 7577113 | Frame_Shift_Del | CA | - | p.144_144del |
| SKCM | TCGA-FS-A4F9-06 | exon_skip_286376 | 7577019 | 7577155 | 7577112 | 7577113 | Frame_Shift_Del | CA | - | p.CA275fs |
| SARC | TCGA-QQ-A5VB-01 | exon_skip_286376 | 7577019 | 7577155 | 7577114 | 7577114 | Frame_Shift_Del | C | - | p.C275fs |
| ESCA | TCGA-VR-A8EO-01 | exon_skip_286376 | 7577019 | 7577155 | 7577115 | 7577115 | Frame_Shift_Del | A | - | p.C275fs |
| OV | TCGA-24-1427-01 | exon_skip_286376 | 7577019 | 7577155 | 7577124 | 7577124 | Frame_Shift_Del | C | - | p.V272fs |
| PAAD | TCGA-FB-AAPQ-01 | exon_skip_286376 | 7577019 | 7577155 | 7577131 | 7577132 | Frame_Shift_Del | GC | - | p.S269fs |
| SARC | TCGA-X6-A8C2-01 | exon_skip_286376 | 7577019 | 7577155 | 7577134 | 7577134 | Frame_Shift_Del | G | - | p.N268fs |
| UCS | TCGA-N6-A4VE-01 | exon_skip_286376 | 7577019 | 7577155 | 7577134 | 7577134 | Frame_Shift_Del | G | - | p.N268fs |
| UCS | TCGA-N6-A4VE-01 | exon_skip_286376 | 7577019 | 7577155 | 7577134 | 7577134 | Frame_Shift_Del | G | - | p.S269fs |
| STAD | TCGA-EQ-8122-01 | exon_skip_286376 | 7577019 | 7577155 | 7577141 | 7577141 | Frame_Shift_Del | C | - | p.G266fs |
| GBM | TCGA-27-2521-01 | exon_skip_286376 | 7577019 | 7577155 | 7577149 | 7577149 | Frame_Shift_Del | A | - | p.N263fs |
| LGG | TCGA-HT-7879-01 | exon_skip_286376 | 7577019 | 7577155 | 7577150 | 7577151 | Frame_Shift_Del | TT | - | p.131_131del |
| LGG | TCGA-HT-7879-01 | exon_skip_286376 | 7577019 | 7577155 | 7577150 | 7577151 | Frame_Shift_Del | TT | - | p.N263fs |
| LIHC | TCGA-CC-5258-01 | exon_skip_286376 | 7577019 | 7577155 | 7577150 | 7577150 | Frame_Shift_Del | T | - | p.N263fs |
| LIHC | TCGA-G3-AAV7-01 | exon_skip_286376 | 7577019 | 7577155 | 7577153 | 7577153 | Frame_Shift_Del | C | - | p.G262fs |
| SARC | TCGA-HB-A43Z-01 | exon_skip_286376 | 7577019 | 7577155 | 7577153 | 7577153 | Frame_Shift_Del | C | - | p.G262fs |
| OV | TCGA-04-1357-01 | exon_skip_286379 | 7578177 | 7578289 | 7578179 | 7578180 | Frame_Shift_Del | CA | - | p.P223fs |
| PAAD | TCGA-F2-A8YN-01 | exon_skip_286379 | 7578177 | 7578289 | 7578180 | 7578190 | Frame_Shift_Del | AGGCGGCTCAT | - | p.220_224del |
| PAAD | TCGA-F2-A8YN-01 | exon_skip_286379 | 7578177 | 7578289 | 7578180 | 7578190 | Frame_Shift_Del | AGGCGGCTCAT | - | p.YEPP220fs |
| STAD | TCGA-CG-4477-01 | exon_skip_286379 | 7578177 | 7578289 | 7578183 | 7578187 | Frame_Shift_Del | CGGCT | - | p.221_223del |
| STAD | TCGA-CG-4477-01 | exon_skip_286379 | 7578177 | 7578289 | 7578183 | 7578187 | Frame_Shift_Del | CGGCT | - | p.E221fs |
| HNSC | TCGA-BB-4224-01 | exon_skip_286379 | 7578177 | 7578289 | 7578192 | 7578193 | Frame_Shift_Del | GG | - | p.P219fs |
| LUAD | TCGA-62-A472-01 | exon_skip_286379 | 7578177 | 7578289 | 7578192 | 7578192 | Frame_Shift_Del | G | - | p.P219fs |
| LUSC | TCGA-18-3409-01 | exon_skip_286379 | 7578177 | 7578289 | 7578200 | 7578221 | Frame_Shift_Del | CCACACTATGTCGAAAAGTGTT | - | p.N210fs |
| SKCM | TCGA-D3-A1QA-06 | exon_skip_286379 | 7578177 | 7578289 | 7578206 | 7578207 | Frame_Shift_Del | TA | - | p.HS214fs |
| HNSC | TCGA-MT-A7BN-01 | exon_skip_286379 | 7578177 | 7578289 | 7578207 | 7578207 | Frame_Shift_Del | A | - | p.H214fs |
| GBM | TCGA-14-0813-01 | exon_skip_286379 | 7578177 | 7578289 | 7578211 | 7578214 | Frame_Shift_Del | CGAA | - | p.F212fs |
| BLCA | TCGA-DK-AA6W-01 | exon_skip_286379 | 7578177 | 7578289 | 7578213 | 7578213 | Frame_Shift_Del | A | - | p.F212fs |
| COAD | TCGA-AA-3560-01 | exon_skip_286379 | 7578177 | 7578289 | 7578213 | 7578214 | Frame_Shift_Del | AA | - | p.212_212del |
| LGG | TCGA-E1-A7Z4-01 | exon_skip_286379 | 7578177 | 7578289 | 7578213 | 7578214 | Frame_Shift_Del | AA | - | p.F212fs |
| LGG | TCGA-P5-A5EZ-01 | exon_skip_286379 | 7578177 | 7578289 | 7578213 | 7578213 | Frame_Shift_Del | A | - | p.F212fs |
| LGG | TCGA-P5-A5EZ-01 | exon_skip_286379 | 7578177 | 7578289 | 7578213 | 7578213 | Frame_Shift_Del | A | - | p.R81fs |
| LUSC | TCGA-18-3407-01 | exon_skip_286379 | 7578177 | 7578289 | 7578213 | 7578214 | Frame_Shift_Del | AA | - | p.F212fs |
| PAAD | TCGA-2J-AABT-01 | exon_skip_286379 | 7578177 | 7578289 | 7578213 | 7578213 | Frame_Shift_Del | A | - | p.F212fs |
| SARC | TCGA-LI-A67I-01 | exon_skip_286379 | 7578177 | 7578289 | 7578213 | 7578213 | Frame_Shift_Del | A | - | p.F212fs |
| SARC | TCGA-LI-A67I-01 | exon_skip_286379 | 7578177 | 7578289 | 7578213 | 7578213 | Frame_Shift_Del | A | - | p.R213fs |
| HNSC | TCGA-CR-7386-01 | exon_skip_286379 | 7578177 | 7578289 | 7578217 | 7578218 | Frame_Shift_Del | GT | - | p.T211fs |
| BRCA | TCGA-AO-A0J6-01 | exon_skip_286379 | 7578177 | 7578289 | 7578218 | 7578218 | Frame_Shift_Del | T | - | p.T211fs |
| OV | TCGA-04-1343-01 | exon_skip_286379 | 7578177 | 7578289 | 7578220 | 7578224 | Frame_Shift_Del | TTTCT | - | p.R209fs |
| BLCA | TCGA-UY-A8OB-01 | exon_skip_286379 | 7578177 | 7578289 | 7578222 | 7578223 | Frame_Shift_Del | TC | - | p.R209fs |
| BRCA | TCGA-A8-A06U-01 | exon_skip_286379 | 7578177 | 7578289 | 7578222 | 7578223 | Frame_Shift_Del | TC | - | p.R209fs |
| BRCA | TCGA-A8-A094-01 | exon_skip_286379 | 7578177 | 7578289 | 7578222 | 7578223 | Frame_Shift_Del | TC | - | p.R209fs |
| ESCA | TCGA-2H-A9GN-01 | exon_skip_286379 | 7578177 | 7578289 | 7578222 | 7578223 | Frame_Shift_Del | TC | - | p.209_210del |
| ESCA | TCGA-2H-A9GN-01 | exon_skip_286379 | 7578177 | 7578289 | 7578222 | 7578223 | Frame_Shift_Del | TC | - | p.R209fs |
| HNSC | TCGA-CN-5358-01 | exon_skip_286379 | 7578177 | 7578289 | 7578222 | 7578223 | Frame_Shift_Del | TC | - | p.R209fs |
| PRAD | TCGA-HC-7742-01 | exon_skip_286379 | 7578177 | 7578289 | 7578222 | 7578223 | Frame_Shift_Del | TC | - | p.77_78del |
| PRAD | TCGA-HC-7742-01 | exon_skip_286379 | 7578177 | 7578289 | 7578222 | 7578223 | Frame_Shift_Del | TC | - | p.R209fs |
| PRAD | TCGA-V1-A9ZI-01 | exon_skip_286379 | 7578177 | 7578289 | 7578222 | 7578223 | Frame_Shift_Del | TC | - | p.R209fs |
| SARC | TCGA-MB-A5YA-01 | exon_skip_286379 | 7578177 | 7578289 | 7578222 | 7578223 | Frame_Shift_Del | TC | - | p.R209fs |
| LUSC | TCGA-46-3769-01 | exon_skip_286379 | 7578177 | 7578289 | 7578230 | 7578230 | Frame_Shift_Del | C | - | p.D207fs |
| HNSC | TCGA-CV-6937-01 | exon_skip_286379 | 7578177 | 7578289 | 7578232 | 7578232 | Frame_Shift_Del | A | - | p.L206fs |
| LIHC | TCGA-DD-A3A0-01 | exon_skip_286379 | 7578177 | 7578289 | 7578232 | 7578232 | Frame_Shift_Del | A | - | p.L206fs |
| HNSC | TCGA-F7-8298-01 | exon_skip_286379 | 7578177 | 7578289 | 7578237 | 7578261 | Frame_Shift_Del | CTCCACACGCAAATTTCCTTCCACT | - | p.RVEGNLRVE196fs |
| LIHC | TCGA-DD-AADN-01 | exon_skip_286379 | 7578177 | 7578289 | 7578237 | 7578238 | Frame_Shift_Del | CT | - | p.204_205del |
| BRCA | TCGA-A2-A0CM-01 | exon_skip_286379 | 7578177 | 7578289 | 7578239 | 7578239 | Frame_Shift_Del | C | - | p.E204fs |
| COAD | TCGA-D5-6534-01 | exon_skip_286379 | 7578177 | 7578289 | 7578240 | 7578241 | Frame_Shift_Del | CA | - | p.71_72del |
| HNSC | TCGA-CV-6950-01 | exon_skip_286379 | 7578177 | 7578289 | 7578241 | 7578241 | Frame_Shift_Del | A | - | p.V203fs |
| PRAD | TCGA-EJ-5525-01 | exon_skip_286379 | 7578177 | 7578289 | 7578242 | 7578242 | Frame_Shift_Del | C | - | p.V203fs |
| HNSC | TCGA-MZ-A7D7-01 | exon_skip_286379 | 7578177 | 7578289 | 7578250 | 7578250 | Frame_Shift_Del | T | - | p.N200fs |
| LGG | TCGA-TM-A84L-01 | exon_skip_286379 | 7578177 | 7578289 | 7578250 | 7578250 | Frame_Shift_Del | T | - | p.N200fs |
| HNSC | TCGA-BB-7870-01 | exon_skip_286379 | 7578177 | 7578289 | 7578255 | 7578255 | Frame_Shift_Del | T | - | p.E198fs |
| HNSC | TCGA-D6-A6EO-01 | exon_skip_286379 | 7578177 | 7578289 | 7578262 | 7578277 | Frame_Shift_Del | CGGATAAGATGCTGAG | - | p.PQHLIR191fs |
| GBM | TCGA-14-0817-01 | exon_skip_286379 | 7578177 | 7578289 | 7578264 | 7578268 | Frame_Shift_Del | GATAA | - | p.L194fs |
| LIHC | TCGA-G3-A7M9-01 | exon_skip_286379 | 7578177 | 7578289 | 7578264 | 7578270 | Frame_Shift_Del | GATAAGA | - | p.194_196del |
| LIHC | TCGA-G3-A7M9-01 | exon_skip_286379 | 7578177 | 7578289 | 7578264 | 7578270 | Frame_Shift_Del | GATAAGA | - | p.HLI193fs |
| BLCA | TCGA-GU-AATP-01 | exon_skip_286379 | 7578177 | 7578289 | 7578267 | 7578283 | Frame_Shift_Del | AAGATGCTGAGGAGGGG | - | p.APPQHL189fs |
| HNSC | TCGA-CQ-6218-01 | exon_skip_286379 | 7578177 | 7578289 | 7578267 | 7578267 | Frame_Shift_Del | A | - | p.L194fs |
| SKCM | TCGA-EE-A2GJ-06 | exon_skip_286379 | 7578177 | 7578289 | 7578267 | 7578267 | Frame_Shift_Del | A | - | p.I63fs |
| SKCM | TCGA-EE-A2GJ-06 | exon_skip_286379 | 7578177 | 7578289 | 7578267 | 7578267 | Frame_Shift_Del | A | - | p.L194fs |
| SARC | TCGA-N1-A6IA-01 | exon_skip_286379 | 7578177 | 7578289 | 7578284 | 7578284 | Frame_Shift_Del | C | - | p.A189fs |
| OV | TCGA-25-1320-01 | exon_skip_286384 | 7579312 | 7579590 | 7579315 | 7579315 | Frame_Shift_Del | G | - | p.C124fs |
| LGG | TCGA-QH-A6X3-01 | exon_skip_286384 | 7579312 | 7579590 | 7579319 | 7579323 | Frame_Shift_Del | GTCAC | - | p.VT122fs |
| BRCA | TCGA-AR-A1AY-01 | exon_skip_286384 | 7579312 | 7579590 | 7579321 | 7579322 | Frame_Shift_Del | CA | - | p.V122fs |
| ESCA | TCGA-LN-A49K-01 | exon_skip_286384 | 7579312 | 7579590 | 7579321 | 7579322 | Frame_Shift_Del | CA | - | p.122_123del |
| ESCA | TCGA-LN-A49K-01 | exon_skip_286384 | 7579312 | 7579590 | 7579321 | 7579322 | Frame_Shift_Del | CA | - | p.V122fs |
| PAAD | TCGA-3A-A9IC-01 | exon_skip_286384 | 7579312 | 7579590 | 7579321 | 7579322 | Frame_Shift_Del | CA | - | p.122_123del |
| PAAD | TCGA-3A-A9IC-01 | exon_skip_286384 | 7579312 | 7579590 | 7579321 | 7579322 | Frame_Shift_Del | CA | - | p.V122fs |
| SARC | TCGA-QQ-A8VF-01 | exon_skip_286384 | 7579312 | 7579590 | 7579321 | 7579322 | Frame_Shift_Del | CA | - | p.V122fs |
| UCS | TCGA-N8-A4PM-01 | exon_skip_286384 | 7579312 | 7579590 | 7579324 | 7579325 | Frame_Shift_Del | AG | - | p.121_122del |
| UCS | TCGA-N8-A4PM-01 | exon_skip_286384 | 7579312 | 7579590 | 7579324 | 7579325 | Frame_Shift_Del | AG | - | p.S121fs |
| LGG | TCGA-TQ-A7RJ-01 | exon_skip_286384 | 7579312 | 7579590 | 7579328 | 7579328 | Frame_Shift_Del | T | - | p.K120fs |
| LUAD | TCGA-86-7953-01 | exon_skip_286384 | 7579312 | 7579590 | 7579329 | 7579345 | Frame_Shift_Del | TGGCTGTCCCAGAATGC | - | p.LHSGTAK114fs |
| HNSC | TCGA-CV-7437-01 | exon_skip_286384 | 7579312 | 7579590 | 7579336 | 7579336 | Frame_Shift_Del | C | - | p.G117fs |
| HNSC | TCGA-CV-6956-01 | exon_skip_286384 | 7579312 | 7579590 | 7579356 | 7579359 | Frame_Shift_Del | GACG | - | p.R110fs |
| HNSC | TCGA-CV-6956-01 | exon_skip_286384 | 7579312 | 7579590 | 7579356 | 7579359 | Frame_Shift_Del | GACG | - | p.RL110fs |
| BRCA | TCGA-AR-A1AN-01 | exon_skip_286384 | 7579312 | 7579590 | 7579359 | 7579359 | Frame_Shift_Del | G | - | p.R110fs |
| BRCA | TCGA-BH-A0C0-01 | exon_skip_286384 | 7579312 | 7579590 | 7579359 | 7579359 | Frame_Shift_Del | G | - | p.R110fs |
| BRCA | TCGA-D8-A27H-01 | exon_skip_286384 | 7579312 | 7579590 | 7579360 | 7579364 | Frame_Shift_Del | GAAAC | - | p.G108fs |
| BRCA | TCGA-A2-A04P-01 | exon_skip_286384 | 7579312 | 7579590 | 7579364 | 7579364 | Frame_Shift_Del | C | - | p.G108fs |
| BRCA | TCGA-A2-A04U-01 | exon_skip_286384 | 7579312 | 7579590 | 7579364 | 7579364 | Frame_Shift_Del | C | - | p.G108fs |
| BRCA | TCGA-AN-A0AJ-01 | exon_skip_286384 | 7579312 | 7579590 | 7579364 | 7579364 | Frame_Shift_Del | C | - | p.G108fs |
| BRCA | TCGA-AR-A1AH-01 | exon_skip_286384 | 7579312 | 7579590 | 7579364 | 7579365 | Frame_Shift_Del | CC | - | p.G108fs |
| LIHC | TCGA-FV-A496-01 | exon_skip_286384 | 7579312 | 7579590 | 7579380 | 7579380 | Frame_Shift_Del | A | - | p.Y103fs |
| STAD | TCGA-BR-8679-01 | exon_skip_286384 | 7579312 | 7579590 | 7579381 | 7579381 | Frame_Shift_Del | G | - | p.T102fs |
| STAD | TCGA-BR-8679-01 | exon_skip_286384 | 7579312 | 7579590 | 7579381 | 7579381 | Frame_Shift_Del | G | - | p.Y103fs |
| LIHC | TCGA-BC-A69H-01 | exon_skip_286384 | 7579312 | 7579590 | 7579389 | 7579399 | Frame_Shift_Del | GGGAAGGGACA | - | p.97_100del |
| HNSC | TCGA-CV-6959-01 | exon_skip_286384 | 7579312 | 7579590 | 7579390 | 7579393 | Frame_Shift_Del | GGAA | - | p.P98fs |
| HNSC | TCGA-CV-6959-01 | exon_skip_286384 | 7579312 | 7579590 | 7579390 | 7579393 | Frame_Shift_Del | GGAA | - | p.PS98fs |
| STAD | TCGA-D7-A74B-01 | exon_skip_286384 | 7579312 | 7579590 | 7579394 | 7579400 | Frame_Shift_Del | GGGACAG | - | p.96_98del |
| STAD | TCGA-D7-A74B-01 | exon_skip_286384 | 7579312 | 7579590 | 7579394 | 7579400 | Frame_Shift_Del | GGGACAG | - | p.SVP96fs |
| SKCM | TCGA-FS-A1Z4-06 | exon_skip_286384 | 7579312 | 7579590 | 7579399 | 7579399 | Frame_Shift_Del | A | - | p.S96fs |
| PRAD | TCGA-KC-A7F6-01 | exon_skip_286384 | 7579312 | 7579590 | 7579402 | 7579418 | Frame_Shift_Del | AGATGACAGGGGCCAGG | - | p.SWPLSS90fs |
| PRAD | TCGA-VP-A87D-01 | exon_skip_286384 | 7579312 | 7579590 | 7579408 | 7579430 | Frame_Shift_Del | CAGGGGCCAGGAGGGGGCTGGTG | - | p.APAPSWPL86fs |
| HNSC | TCGA-CV-5430-01 | exon_skip_286384 | 7579312 | 7579590 | 7579410 | 7579420 | Frame_Shift_Del | GGGGCCAGGAG | - | p.P89fs |
| HNSC | TCGA-CV-5430-01 | exon_skip_286384 | 7579312 | 7579590 | 7579410 | 7579420 | Frame_Shift_Del | GGGGCCAGGAG | - | p.PSWPL89fs |
| LGG | TCGA-TM-A7CA-01 | exon_skip_286384 | 7579312 | 7579590 | 7579420 | 7579420 | Frame_Shift_Del | G | - | p.P89fs |
| LIHC | TCGA-2Y-A9H4-01 | exon_skip_286384 | 7579312 | 7579590 | 7579420 | 7579420 | Frame_Shift_Del | G | - | p.S90fs |
| LUAD | TCGA-86-A4JF-01 | exon_skip_286384 | 7579312 | 7579590 | 7579420 | 7579420 | Frame_Shift_Del | G | - | p.P89fs |
| OV | TCGA-61-2101-01 | exon_skip_286384 | 7579312 | 7579590 | 7579423 | 7579432 | Frame_Shift_Del | GGCTGGTGCA | - | p.P85fs |
| HNSC | TCGA-CR-7364-01 | exon_skip_286384 | 7579312 | 7579590 | 7579433 | 7579433 | Frame_Shift_Del | G | - | p.P85fs |
| HNSC | TCGA-UF-A71D-01 | exon_skip_286384 | 7579312 | 7579590 | 7579437 | 7579437 | Frame_Shift_Del | C | - | p.A84fs |
| HNSC | TCGA-CN-6017-01 | exon_skip_286384 | 7579312 | 7579590 | 7579441 | 7579453 | Frame_Shift_Del | CGGTGTAGGAGCT | - | p.A78fs |
| HNSC | TCGA-CN-6017-01 | exon_skip_286384 | 7579312 | 7579590 | 7579441 | 7579453 | Frame_Shift_Del | CGGTGTAGGAGCT | - | p.AAPTP78fs |
| STAD | TCGA-BR-A4PF-01 | exon_skip_286384 | 7579312 | 7579590 | 7579442 | 7579442 | Frame_Shift_Del | G | - | p.P82fs |
| OV | TCGA-13-1505-01 | exon_skip_286384 | 7579312 | 7579590 | 7579462 | 7579462 | Frame_Shift_Del | A | - | p.P75fs |
| LUAD | TCGA-44-2656-01 | exon_skip_286384 | 7579312 | 7579590 | 7579470 | 7579470 | Frame_Shift_Del | C | - | p.V73fs |
| LUSC | TCGA-60-2713-01 | exon_skip_286384 | 7579312 | 7579590 | 7579470 | 7579470 | Frame_Shift_Del | C | - | p.V73fs |
| BLCA | TCGA-UY-A78N-01 | exon_skip_286384 | 7579312 | 7579590 | 7579471 | 7579471 | Frame_Shift_Del | G | - | p.P72fs |
| LUAD | TCGA-50-5941-01 | exon_skip_286384 | 7579312 | 7579590 | 7579471 | 7579471 | Frame_Shift_Del | G | - | p.P72fs |
| LUAD | TCGA-91-6829-01 | exon_skip_286384 | 7579312 | 7579590 | 7579471 | 7579471 | Frame_Shift_Del | G | - | p.P72fs |
| PAAD | TCGA-3A-A9IU-01 | exon_skip_286384 | 7579312 | 7579590 | 7579471 | 7579471 | Frame_Shift_Del | G | - | p.P72fs |
| PAAD | TCGA-3A-A9IU-01 | exon_skip_286384 | 7579312 | 7579590 | 7579471 | 7579471 | Frame_Shift_Del | G | - | p.V73fs |
| STAD | TCGA-HU-A4H3-01 | exon_skip_286384 | 7579312 | 7579590 | 7579471 | 7579471 | Frame_Shift_Del | G | - | p.V73fs |
| UCEC | TCGA-D1-A17U-01 | exon_skip_286384 | 7579312 | 7579590 | 7579471 | 7579471 | Frame_Shift_Del | G | - | p.P72fs |
| ESCA | TCGA-LN-A5U6-01 | exon_skip_286384 | 7579312 | 7579590 | 7579497 | 7579498 | Frame_Shift_Del | GA | - | p.64_64del |
| ESCA | TCGA-LN-A5U6-01 | exon_skip_286384 | 7579312 | 7579590 | 7579497 | 7579498 | Frame_Shift_Del | GA | - | p.AP63fs |
| ESCA | TCGA-LN-A5U6-01 | exon_skip_286384 | 7579312 | 7579590 | 7579497 | 7579498 | Frame_Shift_Del | GA | - | p.P64fs |
| PAAD | TCGA-2J-AABH-01 | exon_skip_286384 | 7579312 | 7579590 | 7579503 | 7579503 | Frame_Shift_Del | C | - | p.E62fs |
| UCEC | TCGA-FI-A2D2-01 | exon_skip_286384 | 7579312 | 7579590 | 7579505 | 7579506 | Frame_Shift_Del | TC | - | p.D61fs |
| HNSC | TCGA-CN-4728-01 | exon_skip_286384 | 7579312 | 7579590 | 7579514 | 7579514 | Frame_Shift_Del | G | - | p.P58fs |
| HNSC | TCGA-F7-7848-01 | exon_skip_286384 | 7579312 | 7579590 | 7579514 | 7579514 | Frame_Shift_Del | G | - | p.P58fs |
| LIHC | TCGA-DD-AAEI-01 | exon_skip_286384 | 7579312 | 7579590 | 7579521 | 7579521 | Frame_Shift_Del | C | - | p.E56fs |
| LUAD | TCGA-50-6591-01 | exon_skip_286384 | 7579312 | 7579590 | 7579526 | 7579526 | Frame_Shift_Del | A | - | p.F54fs |
| LUSC | TCGA-22-4593-01 | exon_skip_286384 | 7579312 | 7579590 | 7579527 | 7579542 | Frame_Shift_Del | ACCATTGTTCAATATC | - | p.D49fs |
| LUAD | TCGA-64-1677-01 | exon_skip_286384 | 7579312 | 7579590 | 7579536 | 7579545 | Frame_Shift_Del | CAATATCGTC | - | p.D48fs |
| LUAD | TCGA-64-1677-01 | exon_skip_286384 | 7579312 | 7579590 | 7579536 | 7579545 | Frame_Shift_Del | CAATATCGTC | - | p.DDIE48fs |
| BLCA | TCGA-FD-A62N-01 | exon_skip_286384 | 7579312 | 7579590 | 7579544 | 7579556 | Frame_Shift_Del | TCCGGGGACAGCA | - | p.MLSPD44fs |
| LUSC | TCGA-51-4079-01 | exon_skip_286384 | 7579312 | 7579590 | 7579545 | 7579545 | Frame_Shift_Del | C | - | p.D48fs |
| OV | TCGA-25-1329-01 | exon_skip_286384 | 7579312 | 7579590 | 7579547 | 7579547 | Frame_Shift_Del | G | - | p.P47fs |
| OV | TCGA-13-0911-01 | exon_skip_286384 | 7579312 | 7579590 | 7579556 | 7579560 | Frame_Shift_Del | ATCAA | - | p.L43fs |
| LIHC | TCGA-5C-AAPD-01 | exon_skip_286384 | 7579312 | 7579590 | 7579559 | 7579559 | Frame_Shift_Del | A | - | p.L43fs |
| UCEC | TCGA-A5-A0R7-01 | exon_skip_286384 | 7579312 | 7579590 | 7579559 | 7579559 | Frame_Shift_Del | A | - | p.L43fs |
| ESCA | TCGA-VR-A8EY-01 | exon_skip_286384 | 7579312 | 7579590 | 7579563 | 7579563 | Frame_Shift_Del | C | - | p.D42fs |
| HNSC | TCGA-CR-7393-01 | exon_skip_286384 | 7579312 | 7579590 | 7579566 | 7579566 | Frame_Shift_Del | C | - | p.D41fs |
| HNSC | TCGA-CR-7393-01 | exon_skip_286384 | 7579312 | 7579590 | 7579566 | 7579566 | Frame_Shift_Del | C | - | p.D42fs |
| UCS | TCGA-N5-A4RO-01 | exon_skip_286384 | 7579312 | 7579590 | 7579575 | 7579575 | Frame_Shift_Del | G | - | p.Q38fs |
| HNSC | TCGA-CR-7389-01 | exon_skip_286384 | 7579312 | 7579590 | 7579579 | 7579579 | Frame_Shift_Del | C | - | p.P36fs |
| LUAD | TCGA-44-5643-01 | exon_skip_286384 | 7579312 | 7579590 | 7579580 | 7579580 | Frame_Shift_Del | G | - | p.P36fs |
| BLCA | TCGA-XF-AAMJ-01 | exon_skip_286384 | 7579312 | 7579590 | 7579581 | 7579582 | Frame_Shift_Del | GC | - | p.LP35fs |
| LUAD | TCGA-55-7903-01 | exon_skip_286384 | 7579312 | 7579590 | 7579583 | 7579583 | Frame_Shift_Del | A | - | p.L35fs |
| LUSC | TCGA-60-2707-01 | exon_skip_286384 | 7579312 | 7579590 | 7579585 | 7579585 | Frame_Shift_Del | G | - | p.P34fs |
| PAAD | TCGA-FB-A5VM-01 | exon_skip_286384 | 7579312 | 7579590 | 7579585 | 7579585 | Frame_Shift_Del | G | - | p.L35fs |
| PAAD | TCGA-FB-A5VM-01 | exon_skip_286384 | 7579312 | 7579590 | 7579585 | 7579585 | Frame_Shift_Del | G | - | p.P34fs |
| STAD | TCGA-D7-6527-01 | exon_skip_286384 | 7579312 | 7579590 | 7579585 | 7579585 | Frame_Shift_Del | G | - | p.L35fs |
| STAD | TCGA-D7-6527-01 | exon_skip_286384 | 7579312 | 7579590 | 7579585 | 7579585 | Frame_Shift_Del | G | - | p.P34fs |
| STAD | TCGA-HU-8604-01 | exon_skip_286384 | 7579312 | 7579590 | 7579585 | 7579585 | Frame_Shift_Del | G | - | p.L35fs |
| HNSC | TCGA-CQ-A4CH-01 | 7579700 | 7579721 | 7579703 | 7579703 | Frame_Shift_Del | A | - | p.V31fs | |
| ACC | TCGA-OR-A5LE-01 | 7579700 | 7579721 | 7579716 | 7579716 | Frame_Shift_Del | G | - | p.P27fs | |
| KICH | TCGA-KO-8408-01 | 7579700 | 7579721 | 7579716 | 7579716 | Frame_Shift_Del | G | - | p.P27fs | |
| LGG | TCGA-WY-A85C-01 | 7579700 | 7579721 | 7579716 | 7579716 | Frame_Shift_Del | G | - | p.P27fs | |
| PAAD | TCGA-H8-A6C1-01 | 7579700 | 7579721 | 7579716 | 7579716 | Frame_Shift_Del | G | - | p.P27fs | |
| HNSC | TCGA-CV-7091-01 | 7579700 | 7579721 | 7579718 | 7579718 | Frame_Shift_Del | A | - | p.L26fs | |
| UCS | TCGA-N5-A4RA-01 | 7579700 | 7579721 | 7579718 | 7579718 | Frame_Shift_Del | A | - | p.L26fs | |
| UCS | TCGA-N5-A4RA-01 | 7579700 | 7579721 | 7579718 | 7579718 | Frame_Shift_Del | A | - | p.P27fs | |
| OV | TCGA-13-0751-01 | exon_skip_286364 | 7573927 | 7574033 | 7573984 | 7573985 | Frame_Shift_Ins | - | AGGCCTT | p.L348fs |
| LGG | TCGA-QH-A65S-01 | exon_skip_286364 | 7573927 | 7574033 | 7573991 | 7573992 | Frame_Shift_Ins | - | A | p.E346_A347delinsX |
| LGG | TCGA-QH-A65S-01 | exon_skip_286364 | 7573927 | 7574033 | 7573991 | 7573992 | Frame_Shift_Ins | - | A | p.KG345fs |
| STAD | TCGA-D7-6526-01 | exon_skip_286364 | 7573927 | 7574033 | 7573993 | 7573994 | Frame_Shift_Ins | - | TCAGC | p.N345fs |
| STAD | TCGA-D7-6526-01 | exon_skip_286364 | 7573927 | 7574033 | 7573993 | 7573994 | Frame_Shift_Ins | - | TCAGC | p.N345_E346delinsSX |
| STAD | TCGA-D7-6526-01 | exon_skip_286364 | 7573927 | 7574033 | 7573994 | 7573995 | Frame_Shift_Ins | - | TCAGC | p.N345fs |
| LUAD | TCGA-86-8672-01 | exon_skip_286364 | 7573927 | 7574033 | 7574006 | 7574007 | Frame_Shift_Ins | - | CTTC | p.IP340fs |
| ACC | TCGA-OR-A5JP-01 | exon_skip_286364 | 7573927 | 7574033 | 7574011 | 7574012 | Frame_Shift_Ins | - | CGAAG | p.D339fs |
| ACC | TCGA-OR-A5JP-01 | exon_skip_286364 | 7573927 | 7574033 | 7574011 | 7574012 | Frame_Shift_Ins | - | CGAAG | p.E300fs |
| ACC | TCGA-OR-A5JP-01 | exon_skip_286364 | 7573927 | 7574033 | 7574011 | 7574012 | Frame_Shift_Ins | - | CGAAG | p.E339fs |
| HNSC | TCGA-BB-8601-01 | exon_skip_286371 | 7576853 | 7576926 | 7576862 | 7576863 | Frame_Shift_Ins | - | A | p.Y328fs |
| HNSC | TCGA-F7-A61W-01 | exon_skip_286371 | 7576853 | 7576926 | 7576862 | 7576863 | Frame_Shift_Ins | - | A | p.Y328fs |
| LGG | TCGA-DH-A66B-01 | exon_skip_286371 | 7576853 | 7576926 | 7576886 | 7576887 | Frame_Shift_Ins | - | T | p.K188fs |
| LGG | TCGA-DH-A66B-01 | exon_skip_286371 | 7576853 | 7576926 | 7576886 | 7576887 | Frame_Shift_Ins | - | T | p.K320fs |
| HNSC | TCGA-CV-5439-01 | exon_skip_286371 | 7576853 | 7576926 | 7576896 | 7576897 | Frame_Shift_Ins | - | G | p.A317fs |
| HNSC | TCGA-CV-5439-01 | exon_skip_286371 | 7576853 | 7576926 | 7576896 | 7576897 | Frame_Shift_Ins | - | G | p.Q317fs |
| OV | TCGA-24-1603-01 | exon_skip_286371 | 7576853 | 7576926 | 7576900 | 7576901 | Frame_Shift_Ins | - | A | p.S315fs |
| BLCA | TCGA-XF-AAMG-01 | exon_skip_286376 | 7577019 | 7577155 | 7577022 | 7577023 | Frame_Shift_Ins | - | C | p.R306fs |
| GBM | TCGA-14-0871-01 | exon_skip_286376 | 7577019 | 7577155 | 7577035 | 7577036 | Frame_Shift_Ins | - | G | p.P301fs |
| PAAD | TCGA-HZ-7926-01 | exon_skip_286376 | 7577019 | 7577155 | 7577035 | 7577036 | Frame_Shift_Ins | - | G | p.P301fs |
| PAAD | TCGA-HZ-7926-01 | exon_skip_286376 | 7577019 | 7577155 | 7577035 | 7577036 | Frame_Shift_Ins | - | G | p.R301fs |
| SARC | TCGA-DX-A6Z0-01 | exon_skip_286376 | 7577019 | 7577155 | 7577074 | 7577075 | Frame_Shift_Ins | - | TTCTC | p.N288fs |
| SARC | TCGA-DX-A6Z0-01 | exon_skip_286376 | 7577019 | 7577155 | 7577074 | 7577075 | Frame_Shift_Ins | - | TTCTC | p.T288fs |
| LGG | TCGA-HT-7884-01 | exon_skip_286376 | 7577019 | 7577155 | 7577076 | 7577077 | Frame_Shift_Ins | - | C | p.N156fs |
| LGG | TCGA-HT-7884-01 | exon_skip_286376 | 7577019 | 7577155 | 7577076 | 7577077 | Frame_Shift_Ins | - | C | p.S288fs |
| HNSC | TCGA-UF-A7JH-01 | exon_skip_286376 | 7577019 | 7577155 | 7577095 | 7577096 | Frame_Shift_Ins | - | TCTC | p.A281fs |
| BLCA | TCGA-FD-A3SR-01 | exon_skip_286376 | 7577019 | 7577155 | 7577104 | 7577105 | Frame_Shift_Ins | - | GGACAGGC | p.-278fs |
| BLCA | TCGA-FD-A3SR-01 | exon_skip_286376 | 7577019 | 7577155 | 7577104 | 7577105 | Frame_Shift_Ins | - | GGACAGGC | p.P278fs |
| UCEC | TCGA-AX-A0IU-01 | exon_skip_286376 | 7577019 | 7577155 | 7577105 | 7577106 | Frame_Shift_Ins | - | GA | p.P278fs |
| LIHC | TCGA-NI-A8LF-01 | exon_skip_286376 | 7577019 | 7577155 | 7577112 | 7577113 | Frame_Shift_Ins | - | ACAA | p.A276fs |
| BRCA | TCGA-E9-A22G-01 | exon_skip_286376 | 7577019 | 7577155 | 7577127 | 7577128 | Frame_Shift_Ins | - | A | p.E270fs |
| LUSC | TCGA-60-2711-01 | exon_skip_286376 | 7577019 | 7577155 | 7577145 | 7577146 | Frame_Shift_Ins | - | T | p.L264fs |
| LIHC | TCGA-DD-AACZ-01 | exon_skip_286376 | 7577019 | 7577155 | 7577149 | 7577150 | Frame_Shift_Ins | - | C | p.N263fs |
| HNSC | TCGA-BA-7269-01 | exon_skip_286379 | 7578177 | 7578289 | 7578180 | 7578181 | Frame_Shift_Ins | - | T | p.P223fs |
| HNSC | TCGA-BA-7269-01 | exon_skip_286379 | 7578177 | 7578289 | 7578180 | 7578181 | Frame_Shift_Ins | - | T | p.R223fs |
| HNSC | TCGA-DQ-5624-01 | exon_skip_286379 | 7578177 | 7578289 | 7578183 | 7578184 | Frame_Shift_Ins | - | GGCT | p.-221fs |
| HNSC | TCGA-DQ-5624-01 | exon_skip_286379 | 7578177 | 7578289 | 7578183 | 7578184 | Frame_Shift_Ins | - | GGCT | p.P222fs |
| PAAD | TCGA-2J-AABI-01 | exon_skip_286379 | 7578177 | 7578289 | 7578199 | 7578200 | Frame_Shift_Ins | - | CC | p.G217fs |
| PAAD | TCGA-2J-AABI-01 | exon_skip_286379 | 7578177 | 7578289 | 7578199 | 7578200 | Frame_Shift_Ins | - | CC | p.V217fs |
| HNSC | TCGA-HD-7831-01 | exon_skip_286379 | 7578177 | 7578289 | 7578205 | 7578206 | Frame_Shift_Ins | - | T | p.C215fs |
| HNSC | TCGA-HD-7831-01 | exon_skip_286379 | 7578177 | 7578289 | 7578205 | 7578206 | Frame_Shift_Ins | - | T | p.S215fs |
| HNSC | TCGA-CN-6011-01 | exon_skip_286379 | 7578177 | 7578289 | 7578234 | 7578235 | Frame_Shift_Ins | - | T | p.F205fs |
| HNSC | TCGA-CN-6011-01 | exon_skip_286379 | 7578177 | 7578289 | 7578234 | 7578235 | Frame_Shift_Ins | - | T | p.Y205fs |
| BRCA | TCGA-BH-A0BG-01 | exon_skip_286379 | 7578177 | 7578289 | 7578246 | 7578247 | Frame_Shift_Ins | - | A | p.L201fs |
| LUAD | TCGA-38-4629-01 | exon_skip_286379 | 7578177 | 7578289 | 7578246 | 7578247 | Frame_Shift_Ins | - | A | p.S201fs |
| COAD | TCGA-CM-6679-01 | exon_skip_286379 | 7578177 | 7578289 | 7578256 | 7578257 | Frame_Shift_Ins | - | C | p.E198fs |
| STAD | TCGA-BR-A4J8-01 | exon_skip_286379 | 7578177 | 7578289 | 7578266 | 7578267 | Frame_Shift_Ins | - | A | p.I195fs |
| STAD | TCGA-BR-A4J8-01 | exon_skip_286379 | 7578177 | 7578289 | 7578266 | 7578267 | Frame_Shift_Ins | - | A | p.L194fs |
| HNSC | TCGA-CV-7252-01 | exon_skip_286379 | 7578177 | 7578289 | 7578267 | 7578268 | Frame_Shift_Ins | - | AG | p.H194fs |
| HNSC | TCGA-CV-7252-01 | exon_skip_286379 | 7578177 | 7578289 | 7578267 | 7578268 | Frame_Shift_Ins | - | AG | p.L194fs |
| STAD | TCGA-BR-A4J8-01 | exon_skip_286379 | 7578177 | 7578289 | 7578267 | 7578268 | Frame_Shift_Ins | - | A | p.L194fs |
| BRCA | TCGA-E2-A1IO-01 | exon_skip_286379 | 7578177 | 7578289 | 7578278 | 7578279 | Frame_Shift_Ins | - | A | p.P190fs |
| BLCA | TCGA-DK-A1A6-01 | exon_skip_286384 | 7579312 | 7579590 | 7579315 | 7579316 | Frame_Shift_Ins | - | C | p.C124fs |
| BLCA | TCGA-DK-A1A6-06 | exon_skip_286384 | 7579312 | 7579590 | 7579315 | 7579316 | Frame_Shift_Ins | - | C | p.C124fs |
| PAAD | TCGA-IB-AAUP-01 | exon_skip_286384 | 7579312 | 7579590 | 7579315 | 7579316 | Frame_Shift_Ins | - | C | p.Y124fs |
| PRAD | TCGA-KK-A7B4-01 | exon_skip_286384 | 7579312 | 7579590 | 7579315 | 7579316 | Frame_Shift_Ins | - | C | p.C124fs |
| PRAD | TCGA-KK-A7B4-01 | exon_skip_286384 | 7579312 | 7579590 | 7579315 | 7579316 | Frame_Shift_Ins | - | C | p.Y124fs |
| READ | TCGA-G5-6233-01 | exon_skip_286384 | 7579312 | 7579590 | 7579316 | 7579317 | Frame_Shift_Ins | - | AA | p.C124fs |
| PAAD | TCGA-IB-AAUU-01 | exon_skip_286384 | 7579312 | 7579590 | 7579320 | 7579321 | Frame_Shift_Ins | - | C | p.T123fs |
| PAAD | TCGA-IB-AAUU-01 | exon_skip_286384 | 7579312 | 7579590 | 7579320 | 7579321 | Frame_Shift_Ins | - | C | p.VL122fs |
| LGG | TCGA-DB-A75O-01 | exon_skip_286384 | 7579312 | 7579590 | 7579323 | 7579324 | Frame_Shift_Ins | - | A | p.D122fs |
| LGG | TCGA-DU-A7TA-01 | exon_skip_286384 | 7579312 | 7579590 | 7579323 | 7579324 | Frame_Shift_Ins | - | A | p.D122fs |
| SARC | TCGA-DX-A7ET-01 | exon_skip_286384 | 7579312 | 7579590 | 7579328 | 7579329 | Frame_Shift_Ins | - | TAAG | p.K120fs |
| SARC | TCGA-DX-A7ET-01 | exon_skip_286384 | 7579312 | 7579590 | 7579328 | 7579329 | Frame_Shift_Ins | - | TAAG | p.V120fs |
| OV | TCGA-61-2008-01 | exon_skip_286384 | 7579312 | 7579590 | 7579335 | 7579336 | Frame_Shift_Ins | - | C | p.G117fs |
| BRCA | TCGA-AR-A256-01 | exon_skip_286384 | 7579312 | 7579590 | 7579359 | 7579360 | Frame_Shift_Ins | - | GA | p.R109fs |
| BRCA | TCGA-AR-A24K-01 | exon_skip_286384 | 7579312 | 7579590 | 7579360 | 7579361 | Frame_Shift_Ins | - | AA | p.R110fs |
| ESCA | TCGA-L5-A4OR-01 | exon_skip_286384 | 7579312 | 7579590 | 7579377 | 7579378 | Frame_Shift_Ins | - | GT | p.G104fs |
| ESCA | TCGA-L5-A4OR-01 | exon_skip_286384 | 7579312 | 7579590 | 7579377 | 7579378 | Frame_Shift_Ins | - | GT | p.Q103fs |
| ESCA | TCGA-L5-A4OR-01 | exon_skip_286384 | 7579312 | 7579590 | 7579377 | 7579378 | Frame_Shift_Ins | - | GT | p.Q104fs |
| HNSC | TCGA-C9-A47Z-01 | exon_skip_286384 | 7579312 | 7579590 | 7579379 | 7579380 | Frame_Shift_Ins | - | A | p.P103fs |
| STAD | TCGA-BR-8486-01 | exon_skip_286384 | 7579312 | 7579590 | 7579395 | 7579396 | Frame_Shift_Ins | - | C | p.P98fs |
| STAD | TCGA-BR-8486-01 | exon_skip_286384 | 7579312 | 7579590 | 7579395 | 7579396 | Frame_Shift_Ins | - | C | p.V97fs |
| STAD | TCGA-BR-8486-01 | exon_skip_286384 | 7579312 | 7579590 | 7579396 | 7579397 | Frame_Shift_Ins | - | C | p.V97fs |
| READ | TCGA-AF-6136-01 | exon_skip_286384 | 7579312 | 7579590 | 7579406 | 7579407 | Frame_Shift_Ins | - | AC | p.S94fs |
| BLCA | TCGA-GC-A3RB-01 | exon_skip_286384 | 7579312 | 7579590 | 7579413 | 7579414 | Frame_Shift_Ins | - | C | p.P92fs |
| BLCA | TCGA-GC-A3RB-01 | exon_skip_286384 | 7579312 | 7579590 | 7579413 | 7579414 | Frame_Shift_Ins | - | C | p.W91fs |
| HNSC | TCGA-F7-A623-01 | exon_skip_286384 | 7579312 | 7579590 | 7579419 | 7579420 | Frame_Shift_Ins | - | GG | p.L90fs |
| BRCA | TCGA-E2-A1LK-01 | exon_skip_286384 | 7579312 | 7579590 | 7579432 | 7579433 | Frame_Shift_Ins | - | G | p.A86fs |
| HNSC | TCGA-CR-7372-01 | exon_skip_286384 | 7579312 | 7579590 | 7579450 | 7579451 | Frame_Shift_Ins | - | G | p.A79fs |
| BRCA | TCGA-BH-A18Q-01 | exon_skip_286384 | 7579312 | 7579590 | 7579458 | 7579459 | Frame_Shift_Ins | - | TGCA | p.P76fs |
| ACC | TCGA-PK-A5HC-01 | exon_skip_286384 | 7579312 | 7579590 | 7579470 | 7579471 | Frame_Shift_Ins | - | G | p.G73fs |
| ACC | TCGA-PK-A5HC-01 | exon_skip_286384 | 7579312 | 7579590 | 7579470 | 7579471 | Frame_Shift_Ins | - | G | p.V73fs |
| HNSC | TCGA-BA-4076-01 | exon_skip_286384 | 7579312 | 7579590 | 7579470 | 7579471 | Frame_Shift_Ins | - | G | p.G73fs |
| HNSC | TCGA-UF-A7JJ-01 | exon_skip_286384 | 7579312 | 7579590 | 7579470 | 7579471 | Frame_Shift_Ins | - | G | p.G73fs |
| PAAD | TCGA-FB-AAQ1-01 | exon_skip_286384 | 7579312 | 7579590 | 7579470 | 7579471 | Frame_Shift_Ins | - | G | p.G73fs |
| PAAD | TCGA-FB-AAQ1-01 | exon_skip_286384 | 7579312 | 7579590 | 7579470 | 7579471 | Frame_Shift_Ins | - | G | p.V73fs |
| SARC | TCGA-DX-A6B8-01 | exon_skip_286384 | 7579312 | 7579590 | 7579470 | 7579471 | Frame_Shift_Ins | - | G | p.G73fs |
| SARC | TCGA-DX-A6B8-01 | exon_skip_286384 | 7579312 | 7579590 | 7579470 | 7579471 | Frame_Shift_Ins | - | G | p.V72fs |
| STAD | TCGA-HU-A4HD-01 | exon_skip_286384 | 7579312 | 7579590 | 7579470 | 7579471 | Frame_Shift_Ins | - | G | p.P72fs |
| STAD | TCGA-HU-A4HD-01 | exon_skip_286384 | 7579312 | 7579590 | 7579470 | 7579471 | Frame_Shift_Ins | - | G | p.V73fs |
| STAD | TCGA-HU-A4HD-01 | exon_skip_286384 | 7579312 | 7579590 | 7579471 | 7579472 | Frame_Shift_Ins | - | G | p.P72fs |
| LUAD | TCGA-75-6211-01 | exon_skip_286384 | 7579312 | 7579590 | 7579481 | 7579482 | Frame_Shift_Ins | - | C | p.A69fs |
| LUAD | TCGA-75-6211-01 | exon_skip_286384 | 7579312 | 7579590 | 7579481 | 7579482 | Frame_Shift_Ins | - | C | p.C69fs |
| HNSC | TCGA-CN-6021-01 | exon_skip_286384 | 7579312 | 7579590 | 7579494 | 7579495 | Frame_Shift_Ins | - | G | p.N65fs |
| HNSC | TCGA-CN-6021-01 | exon_skip_286384 | 7579312 | 7579590 | 7579494 | 7579495 | Frame_Shift_Ins | - | G | p.P64fs |
| PAAD | TCGA-IB-7886-01 | exon_skip_286384 | 7579312 | 7579590 | 7579518 | 7579519 | Frame_Shift_Ins | - | TT | p.D57fs |
| PAAD | TCGA-IB-7886-01 | exon_skip_286384 | 7579312 | 7579590 | 7579518 | 7579519 | Frame_Shift_Ins | - | TT | p.P57fs |
| STAD | TCGA-KB-A93J-01 | exon_skip_286384 | 7579312 | 7579590 | 7579528 | 7579529 | Frame_Shift_Ins | - | CATT | p.F53fs |
| STAD | TCGA-KB-A93J-01 | exon_skip_286384 | 7579312 | 7579590 | 7579528 | 7579529 | Frame_Shift_Ins | - | CATT | p.W53_F54delinsX |
| READ | TCGA-EI-6885-01 | exon_skip_286384 | 7579312 | 7579590 | 7579530 | 7579531 | Frame_Shift_Ins | - | T | p.W53fs |
| HNSC | TCGA-BA-A6DI-01 | exon_skip_286384 | 7579312 | 7579590 | 7579546 | 7579547 | Frame_Shift_Ins | - | G | p.R47fs |
| ESCA | TCGA-2H-A9GI-01 | exon_skip_286384 | 7579312 | 7579590 | 7579579 | 7579580 | Frame_Shift_Ins | - | GGCAAGGG | p.L36fs |
| ESCA | TCGA-2H-A9GI-01 | exon_skip_286384 | 7579312 | 7579590 | 7579579 | 7579580 | Frame_Shift_Ins | - | GGCAAGGG | p.P36fs |
| LUAD | TCGA-17-Z043-01 | exon_skip_286384 | 7579312 | 7579590 | 7579582 | 7579583 | Frame_Shift_Ins | - | A | p.S35fs |
| LGG | TCGA-FG-6689-01 | exon_skip_286384 | 7579312 | 7579590 | 7579589 | 7579590 | Frame_Shift_Ins | - | A | p.S33fs |
| LUAD | TCGA-44-5645-01 | exon_skip_286364 | 7573927 | 7574033 | 7573967 | 7573967 | Nonsense_Mutation | G | A | p.Q354* |
| LUAD | TCGA-69-7978-01 | exon_skip_286364 | 7573927 | 7574033 | 7573976 | 7573976 | Nonsense_Mutation | T | A | p.K351* |
| LUAD | TCGA-44-8120-01 | exon_skip_286364 | 7573927 | 7574033 | 7573982 | 7573982 | Nonsense_Mutation | C | A | p.E349* |
| LUSC | TCGA-66-2742-01 | exon_skip_286364 | 7573927 | 7574033 | 7573982 | 7573982 | Nonsense_Mutation | C | A | p.E349* |
| UCS | TCGA-N9-A4Q8-01 | exon_skip_286364 | 7573927 | 7574033 | 7573982 | 7573982 | Nonsense_Mutation | C | A | p.E349* |
| UCS | TCGA-N9-A4Q8-01 | exon_skip_286364 | 7573927 | 7574033 | 7573982 | 7573982 | Nonsense_Mutation | C | A | p.E349X |
| LUAD | TCGA-55-7574-01 | exon_skip_286364 | 7573927 | 7574033 | 7573991 | 7573991 | Nonsense_Mutation | C | A | p.E346* |
| ESCA | TCGA-VR-A8EX-01 | exon_skip_286364 | 7573927 | 7574033 | 7574000 | 7574000 | Nonsense_Mutation | C | A | p.E343* |
| ESCA | TCGA-VR-A8EX-01 | exon_skip_286364 | 7573927 | 7574033 | 7574000 | 7574000 | Nonsense_Mutation | C | A | p.E343X |
| HNSC | TCGA-4P-AA8J-01 | exon_skip_286364 | 7573927 | 7574033 | 7574000 | 7574000 | Nonsense_Mutation | C | A | p.E343* |
| LUAD | TCGA-55-8302-01 | exon_skip_286364 | 7573927 | 7574033 | 7574000 | 7574000 | Nonsense_Mutation | C | A | p.E343* |
| LUAD | TCGA-91-6836-01 | exon_skip_286364 | 7573927 | 7574033 | 7574000 | 7574000 | Nonsense_Mutation | C | A | p.E343* |
| LUAD | TCGA-MN-A4N5-01 | exon_skip_286364 | 7573927 | 7574033 | 7574000 | 7574000 | Nonsense_Mutation | C | A | p.E343* |
| BRCA | TCGA-A2-A0YJ-01 | exon_skip_286364 | 7573927 | 7574033 | 7574003 | 7574003 | Nonsense_Mutation | G | A | p.R342* |
| BRCA | TCGA-AN-A0G0-01 | exon_skip_286364 | 7573927 | 7574033 | 7574003 | 7574003 | Nonsense_Mutation | G | A | p.R342* |
| BRCA | TCGA-BH-A0RX-01 | exon_skip_286364 | 7573927 | 7574033 | 7574003 | 7574003 | Nonsense_Mutation | G | A | p.R342* |
| BRCA | TCGA-E2-A1B6-01 | exon_skip_286364 | 7573927 | 7574033 | 7574003 | 7574003 | Nonsense_Mutation | G | A | p.R342* |
| COAD | TCGA-CM-6675-01 | exon_skip_286364 | 7573927 | 7574033 | 7574003 | 7574003 | Nonsense_Mutation | G | A | p.R342X |
| COAD | TCGA-F4-6808-01 | exon_skip_286364 | 7573927 | 7574033 | 7574003 | 7574003 | Nonsense_Mutation | G | A | p.R342X |
| ESCA | TCGA-L5-A891-01 | exon_skip_286364 | 7573927 | 7574033 | 7574003 | 7574003 | Nonsense_Mutation | G | A | p.R342* |
| ESCA | TCGA-L5-A891-01 | exon_skip_286364 | 7573927 | 7574033 | 7574003 | 7574003 | Nonsense_Mutation | G | A | p.R342X |
| ESCA | TCGA-LN-A49S-01 | exon_skip_286364 | 7573927 | 7574033 | 7574003 | 7574003 | Nonsense_Mutation | G | A | p.R342* |
| ESCA | TCGA-LN-A49S-01 | exon_skip_286364 | 7573927 | 7574033 | 7574003 | 7574003 | Nonsense_Mutation | G | A | p.R342X |
| ESCA | TCGA-X8-AAAR-01 | exon_skip_286364 | 7573927 | 7574033 | 7574003 | 7574003 | Nonsense_Mutation | G | A | p.R342* |
| ESCA | TCGA-X8-AAAR-01 | exon_skip_286364 | 7573927 | 7574033 | 7574003 | 7574003 | Nonsense_Mutation | G | A | p.R342X |
| GBM | TCGA-76-4929-01 | exon_skip_286364 | 7573927 | 7574033 | 7574003 | 7574003 | Nonsense_Mutation | G | A | p.R342* |
| HNSC | TCGA-CV-6003-01 | exon_skip_286364 | 7573927 | 7574033 | 7574003 | 7574003 | Nonsense_Mutation | G | A | p.R342* |
| HNSC | TCGA-CV-A468-01 | exon_skip_286364 | 7573927 | 7574033 | 7574003 | 7574003 | Nonsense_Mutation | G | A | p.R342* |
| LGG | TCGA-TM-A7CA-01 | exon_skip_286364 | 7573927 | 7574033 | 7574003 | 7574003 | Nonsense_Mutation | G | A | p.R342* |
| LUAD | TCGA-05-4432-01 | exon_skip_286364 | 7573927 | 7574033 | 7574003 | 7574003 | Nonsense_Mutation | G | A | p.R342* |
| OV | TCGA-13-0884-01 | exon_skip_286364 | 7573927 | 7574033 | 7574003 | 7574003 | Nonsense_Mutation | G | A | p.R342* |
| OV | TCGA-13-1489-01 | exon_skip_286364 | 7573927 | 7574033 | 7574003 | 7574003 | Nonsense_Mutation | G | A | p.R342* |
| OV | TCGA-61-2097-01 | exon_skip_286364 | 7573927 | 7574033 | 7574003 | 7574003 | Nonsense_Mutation | G | A | p.R342* |
| PRAD | TCGA-ZG-A9L0-01 | exon_skip_286364 | 7573927 | 7574033 | 7574003 | 7574003 | Nonsense_Mutation | G | A | p.R342* |
| SARC | TCGA-DX-AB2E-01 | exon_skip_286364 | 7573927 | 7574033 | 7574003 | 7574003 | Nonsense_Mutation | G | A | p.R342* |
| SKCM | TCGA-EB-A431-01 | exon_skip_286364 | 7573927 | 7574033 | 7574003 | 7574003 | Nonsense_Mutation | G | A | p.R342* |
| SKCM | TCGA-EB-A431-01 | exon_skip_286364 | 7573927 | 7574033 | 7574003 | 7574003 | Nonsense_Mutation | G | A | p.R342X |
| SKCM | TCGA-EE-A2GT-06 | exon_skip_286364 | 7573927 | 7574033 | 7574003 | 7574003 | Nonsense_Mutation | G | A | p.R342* |
| SKCM | TCGA-FR-A7U9-06 | exon_skip_286364 | 7573927 | 7574033 | 7574003 | 7574003 | Nonsense_Mutation | G | A | p.R342* |
| SKCM | TCGA-W3-AA1V-06 | exon_skip_286364 | 7573927 | 7574033 | 7574003 | 7574003 | Nonsense_Mutation | G | A | p.R342* |
| STAD | TCGA-BR-8360-01 | exon_skip_286364 | 7573927 | 7574033 | 7574003 | 7574003 | Nonsense_Mutation | G | A | p.R342* |
| STAD | TCGA-IP-7968-01 | exon_skip_286364 | 7573927 | 7574033 | 7574003 | 7574003 | Nonsense_Mutation | G | A | p.R342* |
| STAD | TCGA-IP-7968-01 | exon_skip_286364 | 7573927 | 7574033 | 7574003 | 7574003 | Nonsense_Mutation | G | A | p.R342X |
| UCEC | TCGA-B5-A11E-01 | exon_skip_286364 | 7573927 | 7574033 | 7574003 | 7574003 | Nonsense_Mutation | G | A | p.R342* |
| ACC | TCGA-OR-A5KO-01 | exon_skip_286364 | 7573927 | 7574033 | 7574012 | 7574012 | Nonsense_Mutation | C | A | p.E339* |
| ACC | TCGA-OR-A5KO-01 | exon_skip_286364 | 7573927 | 7574033 | 7574012 | 7574012 | Nonsense_Mutation | C | A | p.E339X |
| HNSC | TCGA-CV-7423-01 | exon_skip_286364 | 7573927 | 7574033 | 7574012 | 7574012 | Nonsense_Mutation | C | A | p.E339* |
| LGG | TCGA-FG-8182-01 | exon_skip_286364 | 7573927 | 7574033 | 7574012 | 7574012 | Nonsense_Mutation | C | A | p.E339* |
| LGG | TCGA-FG-8182-01 | exon_skip_286364 | 7573927 | 7574033 | 7574012 | 7574012 | Nonsense_Mutation | C | A | p.E339X |
| LUAD | TCGA-55-8096-01 | exon_skip_286364 | 7573927 | 7574033 | 7574012 | 7574012 | Nonsense_Mutation | C | A | p.E339* |
| BLCA | TCGA-4Z-AA7R-01 | exon_skip_286364 | 7573927 | 7574033 | 7574021 | 7574021 | Nonsense_Mutation | C | A | p.E336* |
| BLCA | TCGA-FJ-A3Z7-01 | exon_skip_286364 | 7573927 | 7574033 | 7574021 | 7574021 | Nonsense_Mutation | C | A | p.E336* |
| BLCA | TCGA-K4-A6MB-01 | exon_skip_286364 | 7573927 | 7574033 | 7574021 | 7574021 | Nonsense_Mutation | C | A | p.E336* |
| BLCA | TCGA-ZF-A9RN-01 | exon_skip_286364 | 7573927 | 7574033 | 7574021 | 7574021 | Nonsense_Mutation | C | A | p.E336* |
| HNSC | TCGA-DQ-5631-01 | exon_skip_286364 | 7573927 | 7574033 | 7574021 | 7574021 | Nonsense_Mutation | C | A | p.E336* |
| LUAD | TCGA-44-7660-01 | exon_skip_286364 | 7573927 | 7574033 | 7574021 | 7574021 | Nonsense_Mutation | C | A | p.E336* |
| BLCA | TCGA-DK-A6B6-01 | exon_skip_286371 | 7576853 | 7576926 | 7576855 | 7576855 | Nonsense_Mutation | G | A | p.Q331* |
| BLCA | TCGA-G2-A3IB-01 | exon_skip_286371 | 7576853 | 7576926 | 7576855 | 7576855 | Nonsense_Mutation | G | A | p.Q331* |
| BLCA | TCGA-K4-A5RJ-01 | exon_skip_286371 | 7576853 | 7576926 | 7576855 | 7576855 | Nonsense_Mutation | G | A | p.Q331* |
| BLCA | TCGA-KQ-A41S-01 | exon_skip_286371 | 7576853 | 7576926 | 7576855 | 7576855 | Nonsense_Mutation | G | A | p.Q331* |
| BLCA | TCGA-UY-A9PH-01 | exon_skip_286371 | 7576853 | 7576926 | 7576855 | 7576855 | Nonsense_Mutation | G | A | p.Q331* |
| BLCA | TCGA-XF-A9T0-01 | exon_skip_286371 | 7576853 | 7576926 | 7576855 | 7576855 | Nonsense_Mutation | G | A | p.Q331* |
| BLCA | TCGA-ZF-AA5H-01 | exon_skip_286371 | 7576853 | 7576926 | 7576855 | 7576855 | Nonsense_Mutation | G | A | p.Q331* |
| BRCA | TCGA-A2-A0D1-01 | exon_skip_286371 | 7576853 | 7576926 | 7576855 | 7576855 | Nonsense_Mutation | G | A | p.Q331* |
| BRCA | TCGA-BH-A18H-01 | exon_skip_286371 | 7576853 | 7576926 | 7576855 | 7576855 | Nonsense_Mutation | G | A | p.Q331* |
| HNSC | TCGA-CN-4738-01 | exon_skip_286371 | 7576853 | 7576926 | 7576855 | 7576855 | Nonsense_Mutation | G | A | p.Q331* |
| HNSC | TCGA-CV-6942-01 | exon_skip_286371 | 7576853 | 7576926 | 7576855 | 7576855 | Nonsense_Mutation | G | A | p.Q331* |
| LGG | TCGA-S9-A6WG-01 | exon_skip_286371 | 7576853 | 7576926 | 7576855 | 7576855 | Nonsense_Mutation | G | A | p.Q331* |
| LUAD | TCGA-49-6767-01 | exon_skip_286371 | 7576853 | 7576926 | 7576855 | 7576855 | Nonsense_Mutation | G | A | p.Q331* |
| LUAD | TCGA-55-8085-01 | exon_skip_286371 | 7576853 | 7576926 | 7576855 | 7576855 | Nonsense_Mutation | G | A | p.Q331* |
| MESO | TCGA-MQ-A6BR-01 | exon_skip_286371 | 7576853 | 7576926 | 7576855 | 7576855 | Nonsense_Mutation | G | A | p.Q331* |
| SKCM | TCGA-D3-A3C8-06 | exon_skip_286371 | 7576853 | 7576926 | 7576855 | 7576855 | Nonsense_Mutation | G | A | p.Q331* |
| SKCM | TCGA-YD-A9TA-06 | exon_skip_286371 | 7576853 | 7576926 | 7576855 | 7576855 | Nonsense_Mutation | G | A | p.Q331* |
| UCEC | TCGA-BK-A0CC-01 | exon_skip_286371 | 7576853 | 7576926 | 7576855 | 7576855 | Nonsense_Mutation | G | A | p.Q331* |
| SKCM | TCGA-D9-A6EA-06 | exon_skip_286371 | 7576853 | 7576926 | 7576865 | 7576865 | Nonsense_Mutation | A | T | p.Y327* |
| SKCM | TCGA-D9-A6EA-06 | exon_skip_286371 | 7576853 | 7576926 | 7576865 | 7576865 | Nonsense_Mutation | A | T | p.Y327X |
| ESCA | TCGA-R6-A6DQ-01 | exon_skip_286371 | 7576853 | 7576926 | 7576873 | 7576873 | Nonsense_Mutation | C | A | p.G325* |
| ESCA | TCGA-R6-A6DQ-01 | exon_skip_286371 | 7576853 | 7576926 | 7576873 | 7576873 | Nonsense_Mutation | C | A | p.G325X |
| OV | TCGA-24-2271-01 | exon_skip_286371 | 7576853 | 7576926 | 7576885 | 7576885 | Nonsense_Mutation | T | A | p.K321* |
| BLCA | TCGA-XF-AAMW-01 | exon_skip_286371 | 7576853 | 7576926 | 7576891 | 7576891 | Nonsense_Mutation | T | A | p.K319* |
| BLCA | TCGA-LT-A5Z6-01 | exon_skip_286371 | 7576853 | 7576926 | 7576897 | 7576897 | Nonsense_Mutation | G | A | p.Q317* |
| ESCA | TCGA-L5-A88S-01 | exon_skip_286371 | 7576853 | 7576926 | 7576897 | 7576897 | Nonsense_Mutation | G | A | p.Q317* |
| ESCA | TCGA-L5-A88S-01 | exon_skip_286371 | 7576853 | 7576926 | 7576897 | 7576897 | Nonsense_Mutation | G | A | p.Q317X |
| LGG | TCGA-WY-A858-01 | exon_skip_286371 | 7576853 | 7576926 | 7576897 | 7576897 | Nonsense_Mutation | G | A | p.Q317* |
| LUAD | TCGA-55-7576-01 | exon_skip_286371 | 7576853 | 7576926 | 7576897 | 7576897 | Nonsense_Mutation | G | A | p.Q317* |
| LUAD | TCGA-55-8094-01 | exon_skip_286371 | 7576853 | 7576926 | 7576897 | 7576897 | Nonsense_Mutation | G | A | p.Q317* |
| LUAD | TCGA-55-8507-01 | exon_skip_286371 | 7576853 | 7576926 | 7576897 | 7576897 | Nonsense_Mutation | G | A | p.Q317* |
| OV | TCGA-13-0899-01 | exon_skip_286371 | 7576853 | 7576926 | 7576897 | 7576897 | Nonsense_Mutation | G | A | p.Q317* |
| SARC | TCGA-IS-A3K7-01 | exon_skip_286371 | 7576853 | 7576926 | 7576897 | 7576897 | Nonsense_Mutation | G | A | p.Q317* |
| SKCM | TCGA-EE-A2A2-06 | exon_skip_286371 | 7576853 | 7576926 | 7576897 | 7576897 | Nonsense_Mutation | G | A | p.Q317* |
| SKCM | TCGA-EE-A2A2-06 | exon_skip_286371 | 7576853 | 7576926 | 7576897 | 7576897 | Nonsense_Mutation | G | A | p.Q317X |
| SKCM | TCGA-EE-A3JD-06 | exon_skip_286371 | 7576853 | 7576926 | 7576897 | 7576897 | Nonsense_Mutation | G | A | p.Q317* |
| SKCM | TCGA-EE-A3JD-06 | exon_skip_286371 | 7576853 | 7576926 | 7576897 | 7576897 | Nonsense_Mutation | G | A | p.Q317X |
| SKCM | TCGA-FS-A4F2-06 | exon_skip_286371 | 7576853 | 7576926 | 7576897 | 7576897 | Nonsense_Mutation | G | A | p.Q317* |
| SKCM | TCGA-GN-A26C-01 | exon_skip_286371 | 7576853 | 7576926 | 7576897 | 7576897 | Nonsense_Mutation | G | A | p.Q317* |
| SKCM | TCGA-GN-A26C-01 | exon_skip_286371 | 7576853 | 7576926 | 7576897 | 7576897 | Nonsense_Mutation | G | A | p.Q317X |
| STAD | TCGA-CG-4436-01 | exon_skip_286371 | 7576853 | 7576926 | 7576897 | 7576897 | Nonsense_Mutation | G | A | p.Q317* |
| STAD | TCGA-CG-4436-01 | exon_skip_286371 | 7576853 | 7576926 | 7576897 | 7576897 | Nonsense_Mutation | G | A | p.Q317X |
| BRCA | TCGA-AO-A0JL-01 | exon_skip_286376 | 7577019 | 7577155 | 7577022 | 7577022 | Nonsense_Mutation | G | A | p.R306* |
| BRCA | TCGA-D8-A1XA-01 | exon_skip_286376 | 7577019 | 7577155 | 7577022 | 7577022 | Nonsense_Mutation | G | A | p.R306* |
| COAD | TCGA-AA-3524-01 | exon_skip_286376 | 7577019 | 7577155 | 7577022 | 7577022 | Nonsense_Mutation | G | A | p.R306X |
| COAD | TCGA-CK-5916-01 | exon_skip_286376 | 7577019 | 7577155 | 7577022 | 7577022 | Nonsense_Mutation | G | A | p.R306X |
| COAD | TCGA-CM-6169-01 | exon_skip_286376 | 7577019 | 7577155 | 7577022 | 7577022 | Nonsense_Mutation | G | A | p.R306X |
| COAD | TCGA-F4-6856-01 | exon_skip_286376 | 7577019 | 7577155 | 7577022 | 7577022 | Nonsense_Mutation | G | A | p.R306X |
| ESCA | TCGA-JY-A6FD-01 | exon_skip_286376 | 7577019 | 7577155 | 7577022 | 7577022 | Nonsense_Mutation | G | A | p.R306* |
| ESCA | TCGA-JY-A6FD-01 | exon_skip_286376 | 7577019 | 7577155 | 7577022 | 7577022 | Nonsense_Mutation | G | A | p.R306X |
| ESCA | TCGA-JY-A93E-01 | exon_skip_286376 | 7577019 | 7577155 | 7577022 | 7577022 | Nonsense_Mutation | G | A | p.R306* |
| ESCA | TCGA-JY-A93E-01 | exon_skip_286376 | 7577019 | 7577155 | 7577022 | 7577022 | Nonsense_Mutation | G | A | p.R306X |
| ESCA | TCGA-LN-A9FQ-01 | exon_skip_286376 | 7577019 | 7577155 | 7577022 | 7577022 | Nonsense_Mutation | G | A | p.R306* |
| ESCA | TCGA-LN-A9FQ-01 | exon_skip_286376 | 7577019 | 7577155 | 7577022 | 7577022 | Nonsense_Mutation | G | A | p.R306X |
| HNSC | TCGA-CN-6998-01 | exon_skip_286376 | 7577019 | 7577155 | 7577022 | 7577022 | Nonsense_Mutation | G | A | p.R306* |
| HNSC | TCGA-CR-7377-01 | exon_skip_286376 | 7577019 | 7577155 | 7577022 | 7577022 | Nonsense_Mutation | G | A | p.R306* |
| HNSC | TCGA-CV-7255-01 | exon_skip_286376 | 7577019 | 7577155 | 7577022 | 7577022 | Nonsense_Mutation | G | A | p.R306* |
| HNSC | TCGA-CV-7424-01 | exon_skip_286376 | 7577019 | 7577155 | 7577022 | 7577022 | Nonsense_Mutation | G | A | p.R306* |
| HNSC | TCGA-HD-A6HZ-01 | exon_skip_286376 | 7577019 | 7577155 | 7577022 | 7577022 | Nonsense_Mutation | G | A | p.R306* |
| HNSC | TCGA-P3-A6T3-01 | exon_skip_286376 | 7577019 | 7577155 | 7577022 | 7577022 | Nonsense_Mutation | G | A | p.R306* |
| LGG | TCGA-E1-A7YI-01 | exon_skip_286376 | 7577019 | 7577155 | 7577022 | 7577022 | Nonsense_Mutation | G | A | p.R306* |
| LGG | TCGA-HT-8106-01 | exon_skip_286376 | 7577019 | 7577155 | 7577022 | 7577022 | Nonsense_Mutation | G | A | p.R306* |
| LGG | TCGA-HT-8106-01 | exon_skip_286376 | 7577019 | 7577155 | 7577022 | 7577022 | Nonsense_Mutation | G | A | p.R306X |
| LGG | TCGA-TQ-A7RJ-01 | exon_skip_286376 | 7577019 | 7577155 | 7577022 | 7577022 | Nonsense_Mutation | G | A | p.R306* |
| LIHC | TCGA-FV-A3R2-01 | exon_skip_286376 | 7577019 | 7577155 | 7577022 | 7577022 | Nonsense_Mutation | G | A | p.R306* |
| LIHC | TCGA-FV-A3R2-01 | exon_skip_286376 | 7577019 | 7577155 | 7577022 | 7577022 | Nonsense_Mutation | G | A | p.R306X |
| LUSC | TCGA-22-5489-01 | exon_skip_286376 | 7577019 | 7577155 | 7577022 | 7577022 | Nonsense_Mutation | G | A | p.R306* |
| LUSC | TCGA-66-2792-01 | exon_skip_286376 | 7577019 | 7577155 | 7577022 | 7577022 | Nonsense_Mutation | G | A | p.R306* |
| OV | TCGA-04-1331-01 | exon_skip_286376 | 7577019 | 7577155 | 7577022 | 7577022 | Nonsense_Mutation | G | A | p.R306* |
| OV | TCGA-13-1483-01 | exon_skip_286376 | 7577019 | 7577155 | 7577022 | 7577022 | Nonsense_Mutation | G | A | p.R306* |
| OV | TCGA-13-1488-01 | exon_skip_286376 | 7577019 | 7577155 | 7577022 | 7577022 | Nonsense_Mutation | G | A | p.R306* |
| PAAD | TCGA-OE-A75W-01 | exon_skip_286376 | 7577019 | 7577155 | 7577022 | 7577022 | Nonsense_Mutation | G | A | p.R306* |
| PAAD | TCGA-OE-A75W-01 | exon_skip_286376 | 7577019 | 7577155 | 7577022 | 7577022 | Nonsense_Mutation | G | A | p.R306X |
| READ | TCGA-EI-6881-01 | exon_skip_286376 | 7577019 | 7577155 | 7577022 | 7577022 | Nonsense_Mutation | G | A | p.R306X |
| STAD | TCGA-BR-6457-01 | exon_skip_286376 | 7577019 | 7577155 | 7577022 | 7577022 | Nonsense_Mutation | G | A | p.R306* |
| STAD | TCGA-BR-6457-01 | exon_skip_286376 | 7577019 | 7577155 | 7577022 | 7577022 | Nonsense_Mutation | G | A | p.R306X |
| STAD | TCGA-BR-8682-01 | exon_skip_286376 | 7577019 | 7577155 | 7577022 | 7577022 | Nonsense_Mutation | G | A | p.R306* |
| STAD | TCGA-BR-8682-01 | exon_skip_286376 | 7577019 | 7577155 | 7577022 | 7577022 | Nonsense_Mutation | G | A | p.R306X |
| STAD | TCGA-CD-8535-01 | exon_skip_286376 | 7577019 | 7577155 | 7577022 | 7577022 | Nonsense_Mutation | G | A | p.R306* |
| STAD | TCGA-CD-8535-01 | exon_skip_286376 | 7577019 | 7577155 | 7577022 | 7577022 | Nonsense_Mutation | G | A | p.R306X |
| STAD | TCGA-CG-5726-01 | exon_skip_286376 | 7577019 | 7577155 | 7577022 | 7577022 | Nonsense_Mutation | G | A | p.R306* |
| STAD | TCGA-CG-5726-01 | exon_skip_286376 | 7577019 | 7577155 | 7577022 | 7577022 | Nonsense_Mutation | G | A | p.R306X |
| UCEC | TCGA-B5-A11I-01 | exon_skip_286376 | 7577019 | 7577155 | 7577022 | 7577022 | Nonsense_Mutation | G | A | p.R306* |
| HNSC | TCGA-CQ-A4C7-01 | exon_skip_286376 | 7577019 | 7577155 | 7577025 | 7577025 | Nonsense_Mutation | T | A | p.K305* |
| LUSC | TCGA-34-2596-01 | exon_skip_286376 | 7577019 | 7577155 | 7577025 | 7577025 | Nonsense_Mutation | T | A | p.K305* |
| HNSC | TCGA-CN-4727-01 | exon_skip_286376 | 7577019 | 7577155 | 7577046 | 7577046 | Nonsense_Mutation | C | A | p.E298* |
| HNSC | TCGA-CN-5364-01 | exon_skip_286376 | 7577019 | 7577155 | 7577046 | 7577046 | Nonsense_Mutation | C | A | p.E298* |
| HNSC | TCGA-CN-6995-01 | exon_skip_286376 | 7577019 | 7577155 | 7577046 | 7577046 | Nonsense_Mutation | C | A | p.E298* |
| HNSC | TCGA-CN-A63W-01 | exon_skip_286376 | 7577019 | 7577155 | 7577046 | 7577046 | Nonsense_Mutation | C | A | p.E298* |
| HNSC | TCGA-CV-A45U-01 | exon_skip_286376 | 7577019 | 7577155 | 7577046 | 7577046 | Nonsense_Mutation | C | A | p.E298* |
| HNSC | TCGA-CV-A45W-01 | exon_skip_286376 | 7577019 | 7577155 | 7577046 | 7577046 | Nonsense_Mutation | C | A | p.E298* |
| LUAD | TCGA-50-5049-01 | exon_skip_286376 | 7577019 | 7577155 | 7577046 | 7577046 | Nonsense_Mutation | C | A | p.E298* |
| LUAD | TCGA-99-8033-01 | exon_skip_286376 | 7577019 | 7577155 | 7577046 | 7577046 | Nonsense_Mutation | C | A | p.E298* |
| LUAD | TCGA-O1-A52J-01 | exon_skip_286376 | 7577019 | 7577155 | 7577046 | 7577046 | Nonsense_Mutation | C | A | p.E298* |
| LUSC | TCGA-18-3411-01 | exon_skip_286376 | 7577019 | 7577155 | 7577046 | 7577046 | Nonsense_Mutation | C | A | p.E298* |
| LUSC | TCGA-22-5473-01 | exon_skip_286376 | 7577019 | 7577155 | 7577046 | 7577046 | Nonsense_Mutation | C | A | p.E298* |
| LUSC | TCGA-33-4533-01 | exon_skip_286376 | 7577019 | 7577155 | 7577046 | 7577046 | Nonsense_Mutation | C | A | p.E298* |
| PAAD | TCGA-IB-7889-01 | exon_skip_286376 | 7577019 | 7577155 | 7577046 | 7577046 | Nonsense_Mutation | C | A | p.E298* |
| PAAD | TCGA-IB-7889-01 | exon_skip_286376 | 7577019 | 7577155 | 7577046 | 7577046 | Nonsense_Mutation | C | A | p.E298X |
| PRAD | TCGA-ZG-A9M4-01 | exon_skip_286376 | 7577019 | 7577155 | 7577046 | 7577046 | Nonsense_Mutation | C | A | p.E298* |
| SARC | TCGA-QQ-A5V9-01 | exon_skip_286376 | 7577019 | 7577155 | 7577046 | 7577046 | Nonsense_Mutation | C | A | p.E298* |
| BLCA | TCGA-LC-A66R-01 | exon_skip_286376 | 7577019 | 7577155 | 7577058 | 7577058 | Nonsense_Mutation | C | A | p.E294* |
| BLCA | TCGA-ZF-AA51-01 | exon_skip_286376 | 7577019 | 7577155 | 7577058 | 7577058 | Nonsense_Mutation | C | A | p.E294* |
| ESCA | TCGA-LN-A4A3-01 | exon_skip_286376 | 7577019 | 7577155 | 7577058 | 7577058 | Nonsense_Mutation | C | A | p.E294* |
| ESCA | TCGA-LN-A4A3-01 | exon_skip_286376 | 7577019 | 7577155 | 7577058 | 7577058 | Nonsense_Mutation | C | A | p.E294X |
| ESCA | TCGA-LN-A9FP-01 | exon_skip_286376 | 7577019 | 7577155 | 7577058 | 7577058 | Nonsense_Mutation | C | A | p.E294* |
| ESCA | TCGA-LN-A9FP-01 | exon_skip_286376 | 7577019 | 7577155 | 7577058 | 7577058 | Nonsense_Mutation | C | A | p.E294X |
| HNSC | TCGA-CN-4742-01 | exon_skip_286376 | 7577019 | 7577155 | 7577058 | 7577058 | Nonsense_Mutation | C | A | p.E294* |
| HNSC | TCGA-CQ-A4C6-01 | exon_skip_286376 | 7577019 | 7577155 | 7577058 | 7577058 | Nonsense_Mutation | C | A | p.E294* |
| HNSC | TCGA-QK-A8ZB-01 | exon_skip_286376 | 7577019 | 7577155 | 7577058 | 7577058 | Nonsense_Mutation | C | A | p.E294* |
| LUAD | TCGA-86-7701-01 | exon_skip_286376 | 7577019 | 7577155 | 7577058 | 7577058 | Nonsense_Mutation | C | A | p.E294* |
| PAAD | TCGA-3E-AAAY-01 | exon_skip_286376 | 7577019 | 7577155 | 7577058 | 7577058 | Nonsense_Mutation | C | A | p.E294* |
| PAAD | TCGA-3E-AAAY-01 | exon_skip_286376 | 7577019 | 7577155 | 7577058 | 7577058 | Nonsense_Mutation | C | A | p.E294X |
| KICH | TCGA-KL-8341-01 | exon_skip_286376 | 7577019 | 7577155 | 7577064 | 7577064 | Nonsense_Mutation | T | A | p.K292* |
| KICH | TCGA-KL-8341-01 | exon_skip_286376 | 7577019 | 7577155 | 7577064 | 7577064 | Nonsense_Mutation | T | A | p.K292X |
| LIHC | TCGA-RC-A6M6-01 | exon_skip_286376 | 7577019 | 7577155 | 7577064 | 7577064 | Nonsense_Mutation | T | A | p.K292* |
| LIHC | TCGA-RC-A6M6-01 | exon_skip_286376 | 7577019 | 7577155 | 7577064 | 7577064 | Nonsense_Mutation | T | A | p.K292X |
| BLCA | TCGA-FD-A3SL-01 | exon_skip_286376 | 7577019 | 7577155 | 7577079 | 7577079 | Nonsense_Mutation | C | A | p.E287* |
| BLCA | TCGA-ZF-AA54-01 | exon_skip_286376 | 7577019 | 7577155 | 7577079 | 7577079 | Nonsense_Mutation | C | A | p.E287* |
| LUSC | TCGA-66-2782-01 | exon_skip_286376 | 7577019 | 7577155 | 7577079 | 7577079 | Nonsense_Mutation | C | A | p.E287* |
| READ | TCGA-DT-5265-01 | exon_skip_286376 | 7577019 | 7577155 | 7577079 | 7577079 | Nonsense_Mutation | C | A | p.E287X |
| BLCA | TCGA-GC-A3WC-01 | exon_skip_286376 | 7577019 | 7577155 | 7577082 | 7577082 | Nonsense_Mutation | C | A | p.E286* |
| HNSC | TCGA-CX-A4AQ-01 | exon_skip_286376 | 7577019 | 7577155 | 7577082 | 7577082 | Nonsense_Mutation | C | A | p.E286* |
| LUAD | TCGA-44-2668-01 | exon_skip_286376 | 7577019 | 7577155 | 7577082 | 7577082 | Nonsense_Mutation | C | A | p.E286* |
| PAAD | TCGA-RB-AA9M-01 | exon_skip_286376 | 7577019 | 7577155 | 7577082 | 7577082 | Nonsense_Mutation | C | A | p.E286* |
| PAAD | TCGA-RB-AA9M-01 | exon_skip_286376 | 7577019 | 7577155 | 7577082 | 7577082 | Nonsense_Mutation | C | A | p.E286X |
| BLCA | TCGA-UY-A9PE-01 | exon_skip_286376 | 7577019 | 7577155 | 7577085 | 7577085 | Nonsense_Mutation | C | A | p.E285* |
| COAD | TCGA-A6-6654-01 | exon_skip_286376 | 7577019 | 7577155 | 7577085 | 7577085 | Nonsense_Mutation | C | A | p.E285X |
| HNSC | TCGA-QK-A6IG-01 | exon_skip_286376 | 7577019 | 7577155 | 7577085 | 7577085 | Nonsense_Mutation | C | A | p.E285* |
| LUAD | TCGA-50-5944-01 | exon_skip_286376 | 7577019 | 7577155 | 7577085 | 7577085 | Nonsense_Mutation | C | A | p.E285* |
| STAD | TCGA-B7-A5TI-01 | exon_skip_286376 | 7577019 | 7577155 | 7577085 | 7577085 | Nonsense_Mutation | C | A | p.E285* |
| STAD | TCGA-B7-A5TI-01 | exon_skip_286376 | 7577019 | 7577155 | 7577085 | 7577085 | Nonsense_Mutation | C | A | p.E285X |
| BRCA | TCGA-C8-A1HK-01 | exon_skip_286376 | 7577019 | 7577155 | 7577100 | 7577100 | Nonsense_Mutation | T | A | p.R280* |
| BLCA | TCGA-BT-A20N-01 | exon_skip_286376 | 7577019 | 7577155 | 7577107 | 7577107 | Nonsense_Mutation | A | T | p.C277* |
| LIHC | TCGA-CC-5263-01 | exon_skip_286376 | 7577019 | 7577155 | 7577107 | 7577107 | Nonsense_Mutation | A | T | p.C277* |
| LIHC | TCGA-CC-5263-01 | exon_skip_286376 | 7577019 | 7577155 | 7577107 | 7577107 | Nonsense_Mutation | A | T | p.C277X |
| LIHC | TCGA-DD-A1EE-01 | exon_skip_286376 | 7577019 | 7577155 | 7577107 | 7577107 | Nonsense_Mutation | A | T | p.C277X |
| SKCM | TCGA-WE-A8ZX-06 | exon_skip_286376 | 7577019 | 7577155 | 7577113 | 7577113 | Nonsense_Mutation | A | T | p.C275* |
| LUSC | TCGA-39-5019-01 | exon_skip_286376 | 7577019 | 7577155 | 7577127 | 7577127 | Nonsense_Mutation | C | A | p.E271* |
| OV | TCGA-24-1471-01 | exon_skip_286376 | 7577019 | 7577155 | 7577127 | 7577127 | Nonsense_Mutation | C | A | p.E271* |
| HNSC | TCGA-CN-A497-01 | exon_skip_286376 | 7577019 | 7577155 | 7577142 | 7577142 | Nonsense_Mutation | C | A | p.G266* |
| HNSC | TCGA-CV-6960-01 | exon_skip_286376 | 7577019 | 7577155 | 7577142 | 7577142 | Nonsense_Mutation | C | A | p.G266* |
| HNSC | TCGA-CV-6960-01 | exon_skip_286376 | 7577019 | 7577155 | 7577142 | 7577143 | Nonsense_Mutation | CC | AA | p.G266* |
| LUAD | TCGA-17-Z026-01 | exon_skip_286376 | 7577019 | 7577155 | 7577142 | 7577142 | Nonsense_Mutation | C | A | p.G266* |
| BLCA | TCGA-DK-AA74-01 | exon_skip_286379 | 7578177 | 7578289 | 7578179 | 7578179 | Nonsense_Mutation | C | A | p.E224* |
| ESCA | TCGA-LN-A7HY-01 | exon_skip_286379 | 7578177 | 7578289 | 7578179 | 7578179 | Nonsense_Mutation | C | A | p.E224* |
| ESCA | TCGA-LN-A7HY-01 | exon_skip_286379 | 7578177 | 7578289 | 7578179 | 7578179 | Nonsense_Mutation | C | A | p.E224X |
| STAD | TCGA-VQ-AA68-01 | exon_skip_286379 | 7578177 | 7578289 | 7578179 | 7578179 | Nonsense_Mutation | C | A | p.E224* |
| STAD | TCGA-VQ-AA68-01 | exon_skip_286379 | 7578177 | 7578289 | 7578179 | 7578179 | Nonsense_Mutation | C | A | p.E224X |
| BLCA | TCGA-DK-A1AB-01 | exon_skip_286379 | 7578177 | 7578289 | 7578188 | 7578188 | Nonsense_Mutation | C | A | p.E221* |
| BRCA | TCGA-A7-A13D-01 | exon_skip_286379 | 7578177 | 7578289 | 7578188 | 7578188 | Nonsense_Mutation | C | A | p.E221* |
| HNSC | TCGA-H7-8502-01 | exon_skip_286379 | 7578177 | 7578289 | 7578188 | 7578188 | Nonsense_Mutation | C | A | p.E221* |
| LIHC | TCGA-CC-A7IG-01 | exon_skip_286379 | 7578177 | 7578289 | 7578188 | 7578188 | Nonsense_Mutation | C | A | p.E221* |
| LIHC | TCGA-CC-A7IG-01 | exon_skip_286379 | 7578177 | 7578289 | 7578188 | 7578188 | Nonsense_Mutation | C | A | p.E221X |
| LUSC | TCGA-22-5492-01 | exon_skip_286379 | 7578177 | 7578289 | 7578188 | 7578188 | Nonsense_Mutation | C | A | p.E221* |
| ACC | TCGA-OR-A5LJ-01 | exon_skip_286379 | 7578177 | 7578289 | 7578212 | 7578212 | Nonsense_Mutation | G | A | p.R213* |
| ACC | TCGA-OR-A5LJ-01 | exon_skip_286379 | 7578177 | 7578289 | 7578212 | 7578212 | Nonsense_Mutation | G | A | p.R213X |
| BRCA | TCGA-AO-A0JB-01 | exon_skip_286379 | 7578177 | 7578289 | 7578212 | 7578212 | Nonsense_Mutation | G | A | p.R213* |
| BRCA | TCGA-AO-A124-01 | exon_skip_286379 | 7578177 | 7578289 | 7578212 | 7578212 | Nonsense_Mutation | G | A | p.R213* |
| BRCA | TCGA-B6-A0IQ-01 | exon_skip_286379 | 7578177 | 7578289 | 7578212 | 7578212 | Nonsense_Mutation | G | A | p.R213* |
| BRCA | TCGA-BH-A202-01 | exon_skip_286379 | 7578177 | 7578289 | 7578212 | 7578212 | Nonsense_Mutation | G | A | p.R213* |
| BRCA | TCGA-D8-A1Y3-01 | exon_skip_286379 | 7578177 | 7578289 | 7578212 | 7578212 | Nonsense_Mutation | G | A | p.R213* |
| BRCA | TCGA-E2-A14X-01 | exon_skip_286379 | 7578177 | 7578289 | 7578212 | 7578212 | Nonsense_Mutation | G | A | p.R213* |
| BRCA | TCGA-EW-A1PA-01 | exon_skip_286379 | 7578177 | 7578289 | 7578212 | 7578212 | Nonsense_Mutation | G | A | p.R213* |
| COAD | TCGA-AA-3553-01 | exon_skip_286379 | 7578177 | 7578289 | 7578212 | 7578212 | Nonsense_Mutation | G | A | p.R213X |
| COAD | TCGA-AD-6965-01 | exon_skip_286379 | 7578177 | 7578289 | 7578212 | 7578212 | Nonsense_Mutation | G | A | p.R213X |
| COAD | TCGA-AY-5543-01 | exon_skip_286379 | 7578177 | 7578289 | 7578212 | 7578212 | Nonsense_Mutation | G | A | p.R213X |
| COAD | TCGA-G4-6303-01 | exon_skip_286379 | 7578177 | 7578289 | 7578212 | 7578212 | Nonsense_Mutation | G | A | p.R213X |
| COAD | TCGA-G4-6314-01 | exon_skip_286379 | 7578177 | 7578289 | 7578212 | 7578212 | Nonsense_Mutation | G | A | p.R213X |
| COAD | TCGA-G4-6586-01 | exon_skip_286379 | 7578177 | 7578289 | 7578212 | 7578212 | Nonsense_Mutation | G | A | p.R213X |
| ESCA | TCGA-2H-A9GH-01 | exon_skip_286379 | 7578177 | 7578289 | 7578212 | 7578212 | Nonsense_Mutation | G | A | p.R213* |
| ESCA | TCGA-2H-A9GH-01 | exon_skip_286379 | 7578177 | 7578289 | 7578212 | 7578212 | Nonsense_Mutation | G | A | p.R213X |
| ESCA | TCGA-IG-A4QS-01 | exon_skip_286379 | 7578177 | 7578289 | 7578212 | 7578212 | Nonsense_Mutation | G | A | p.R213* |
| ESCA | TCGA-IG-A4QS-01 | exon_skip_286379 | 7578177 | 7578289 | 7578212 | 7578212 | Nonsense_Mutation | G | A | p.R213X |
| ESCA | TCGA-LN-A49M-01 | exon_skip_286379 | 7578177 | 7578289 | 7578212 | 7578212 | Nonsense_Mutation | G | A | p.R213* |
| ESCA | TCGA-LN-A49M-01 | exon_skip_286379 | 7578177 | 7578289 | 7578212 | 7578212 | Nonsense_Mutation | G | A | p.R213X |
| ESCA | TCGA-XP-A8T6-01 | exon_skip_286379 | 7578177 | 7578289 | 7578212 | 7578212 | Nonsense_Mutation | G | A | p.R213* |
| ESCA | TCGA-XP-A8T6-01 | exon_skip_286379 | 7578177 | 7578289 | 7578212 | 7578212 | Nonsense_Mutation | G | A | p.R213X |
| HNSC | TCGA-BB-4227-01 | exon_skip_286379 | 7578177 | 7578289 | 7578212 | 7578212 | Nonsense_Mutation | G | A | p.R213* |
| HNSC | TCGA-CQ-6222-01 | exon_skip_286379 | 7578177 | 7578289 | 7578212 | 7578212 | Nonsense_Mutation | G | A | p.R213* |
| HNSC | TCGA-CQ-6229-01 | exon_skip_286379 | 7578177 | 7578289 | 7578212 | 7578212 | Nonsense_Mutation | G | A | p.R213* |
| HNSC | TCGA-CV-5434-01 | exon_skip_286379 | 7578177 | 7578289 | 7578212 | 7578212 | Nonsense_Mutation | G | A | p.R213* |
| HNSC | TCGA-CV-6942-01 | exon_skip_286379 | 7578177 | 7578289 | 7578212 | 7578212 | Nonsense_Mutation | G | A | p.R213* |
| HNSC | TCGA-CV-7438-01 | exon_skip_286379 | 7578177 | 7578289 | 7578212 | 7578212 | Nonsense_Mutation | G | A | p.R213* |
| HNSC | TCGA-CX-7082-01 | exon_skip_286379 | 7578177 | 7578289 | 7578212 | 7578212 | Nonsense_Mutation | G | A | p.R213* |
| HNSC | TCGA-IQ-A61O-01 | exon_skip_286379 | 7578177 | 7578289 | 7578212 | 7578212 | Nonsense_Mutation | G | A | p.R213* |
| HNSC | TCGA-UF-A7JD-01 | exon_skip_286379 | 7578177 | 7578289 | 7578212 | 7578212 | Nonsense_Mutation | G | A | p.R213* |
| KICH | TCGA-KN-8431-01 | exon_skip_286379 | 7578177 | 7578289 | 7578212 | 7578212 | Nonsense_Mutation | G | A | p.R213* |
| KICH | TCGA-KO-8413-01 | exon_skip_286379 | 7578177 | 7578289 | 7578212 | 7578212 | Nonsense_Mutation | G | A | p.R213* |
| KICH | TCGA-KO-8413-01 | exon_skip_286379 | 7578177 | 7578289 | 7578212 | 7578212 | Nonsense_Mutation | G | A | p.R213X |
| KICH | TCGA-KO-8416-01 | exon_skip_286379 | 7578177 | 7578289 | 7578212 | 7578212 | Nonsense_Mutation | G | A | p.R213* |
| KICH | TCGA-KO-8416-01 | exon_skip_286379 | 7578177 | 7578289 | 7578212 | 7578212 | Nonsense_Mutation | G | A | p.R213X |
| KIRC | TCGA-B0-5098-01 | exon_skip_286379 | 7578177 | 7578289 | 7578212 | 7578212 | Nonsense_Mutation | G | A | p.R213* |
| LGG | TCGA-HT-7602-01 | exon_skip_286379 | 7578177 | 7578289 | 7578212 | 7578212 | Nonsense_Mutation | G | A | p.R213* |
| LGG | TCGA-HT-7602-01 | exon_skip_286379 | 7578177 | 7578289 | 7578212 | 7578212 | Nonsense_Mutation | G | A | p.R213X |
| LGG | TCGA-HT-8018-01 | exon_skip_286379 | 7578177 | 7578289 | 7578212 | 7578212 | Nonsense_Mutation | G | A | p.R213* |
| LGG | TCGA-HT-8018-01 | exon_skip_286379 | 7578177 | 7578289 | 7578212 | 7578212 | Nonsense_Mutation | G | A | p.R213X |
| LGG | TCGA-HT-A74J-01 | exon_skip_286379 | 7578177 | 7578289 | 7578212 | 7578212 | Nonsense_Mutation | G | A | p.R213* |
| LUAD | TCGA-17-Z020-01 | exon_skip_286379 | 7578177 | 7578289 | 7578212 | 7578212 | Nonsense_Mutation | G | A | p.R213* |
| LUAD | TCGA-44-7661-01 | exon_skip_286379 | 7578177 | 7578289 | 7578212 | 7578212 | Nonsense_Mutation | G | A | p.R213* |
| LUAD | TCGA-49-4490-01 | exon_skip_286379 | 7578177 | 7578289 | 7578212 | 7578212 | Nonsense_Mutation | G | A | p.R213* |
| LUAD | TCGA-55-8510-01 | exon_skip_286379 | 7578177 | 7578289 | 7578212 | 7578212 | Nonsense_Mutation | G | A | p.R213* |
| LUSC | TCGA-39-5029-01 | exon_skip_286379 | 7578177 | 7578289 | 7578212 | 7578212 | Nonsense_Mutation | G | A | p.R213* |
| LUSC | TCGA-56-5897-01 | exon_skip_286379 | 7578177 | 7578289 | 7578212 | 7578212 | Nonsense_Mutation | G | A | p.R213* |
| LUSC | TCGA-60-2698-01 | exon_skip_286379 | 7578177 | 7578289 | 7578212 | 7578212 | Nonsense_Mutation | G | A | p.R213* |
| OV | TCGA-13-0887-01 | exon_skip_286379 | 7578177 | 7578289 | 7578212 | 7578212 | Nonsense_Mutation | G | A | p.R213* |
| PAAD | TCGA-FB-AAPZ-01 | exon_skip_286379 | 7578177 | 7578289 | 7578212 | 7578212 | Nonsense_Mutation | G | A | p.R213* |
| PAAD | TCGA-FB-AAPZ-01 | exon_skip_286379 | 7578177 | 7578289 | 7578212 | 7578212 | Nonsense_Mutation | G | A | p.R213X |
| PAAD | TCGA-LB-A7SX-01 | exon_skip_286379 | 7578177 | 7578289 | 7578212 | 7578212 | Nonsense_Mutation | G | A | p.R213* |
| PAAD | TCGA-LB-A7SX-01 | exon_skip_286379 | 7578177 | 7578289 | 7578212 | 7578212 | Nonsense_Mutation | G | A | p.R213X |
| PAAD | TCGA-LB-A9Q5-01 | exon_skip_286379 | 7578177 | 7578289 | 7578212 | 7578212 | Nonsense_Mutation | G | A | p.R213* |
| PAAD | TCGA-LB-A9Q5-01 | exon_skip_286379 | 7578177 | 7578289 | 7578212 | 7578212 | Nonsense_Mutation | G | A | p.R213X |
| READ | TCGA-AG-3594-01 | exon_skip_286379 | 7578177 | 7578289 | 7578212 | 7578212 | Nonsense_Mutation | G | A | p.R213X |
| READ | TCGA-EI-6917-01 | exon_skip_286379 | 7578177 | 7578289 | 7578212 | 7578212 | Nonsense_Mutation | G | A | p.R213X |
| READ | TCGA-F5-6814-01 | exon_skip_286379 | 7578177 | 7578289 | 7578212 | 7578212 | Nonsense_Mutation | G | A | p.R213X |
| SARC | TCGA-DX-A2J1-01 | exon_skip_286379 | 7578177 | 7578289 | 7578212 | 7578212 | Nonsense_Mutation | G | A | p.R213* |
| SARC | TCGA-DX-A8BV-01 | exon_skip_286379 | 7578177 | 7578289 | 7578212 | 7578212 | Nonsense_Mutation | G | A | p.R213* |
| SKCM | TCGA-D9-A6EC-06 | exon_skip_286379 | 7578177 | 7578289 | 7578212 | 7578212 | Nonsense_Mutation | G | A | p.R213* |
| SKCM | TCGA-D9-A6EC-06 | exon_skip_286379 | 7578177 | 7578289 | 7578212 | 7578212 | Nonsense_Mutation | G | A | p.R213X |
| SKCM | TCGA-EB-A5FP-01 | exon_skip_286379 | 7578177 | 7578289 | 7578212 | 7578212 | Nonsense_Mutation | G | A | p.R213* |
| SKCM | TCGA-EE-A3AE-06 | exon_skip_286379 | 7578177 | 7578289 | 7578212 | 7578212 | Nonsense_Mutation | G | A | p.R213* |
| SKCM | TCGA-EE-A3AE-06 | exon_skip_286379 | 7578177 | 7578289 | 7578212 | 7578212 | Nonsense_Mutation | G | A | p.R213X |
| SKCM | TCGA-EE-A3AG-06 | exon_skip_286379 | 7578177 | 7578289 | 7578212 | 7578212 | Nonsense_Mutation | G | A | p.R213* |
| SKCM | TCGA-EE-A3AG-06 | exon_skip_286379 | 7578177 | 7578289 | 7578212 | 7578212 | Nonsense_Mutation | G | A | p.R213X |
| SKCM | TCGA-W3-AA1R-06 | exon_skip_286379 | 7578177 | 7578289 | 7578212 | 7578212 | Nonsense_Mutation | G | A | p.R213* |
| SKCM | TCGA-Z2-A8RT-06 | exon_skip_286379 | 7578177 | 7578289 | 7578212 | 7578212 | Nonsense_Mutation | G | A | p.R213* |
| STAD | TCGA-BR-7197-01 | exon_skip_286379 | 7578177 | 7578289 | 7578212 | 7578212 | Nonsense_Mutation | G | A | p.R213* |
| STAD | TCGA-BR-7197-01 | exon_skip_286379 | 7578177 | 7578289 | 7578212 | 7578212 | Nonsense_Mutation | G | A | p.R213X |
| STAD | TCGA-CD-8524-01 | exon_skip_286379 | 7578177 | 7578289 | 7578212 | 7578212 | Nonsense_Mutation | G | A | p.R213* |
| STAD | TCGA-CD-8524-01 | exon_skip_286379 | 7578177 | 7578289 | 7578212 | 7578212 | Nonsense_Mutation | G | A | p.R213X |
| STAD | TCGA-CG-4438-01 | exon_skip_286379 | 7578177 | 7578289 | 7578212 | 7578212 | Nonsense_Mutation | G | A | p.R213* |
| STAD | TCGA-CG-4438-01 | exon_skip_286379 | 7578177 | 7578289 | 7578212 | 7578212 | Nonsense_Mutation | G | A | p.R213X |
| STAD | TCGA-CG-4469-01 | exon_skip_286379 | 7578177 | 7578289 | 7578212 | 7578212 | Nonsense_Mutation | G | A | p.R213* |
| STAD | TCGA-CG-4469-01 | exon_skip_286379 | 7578177 | 7578289 | 7578212 | 7578212 | Nonsense_Mutation | G | A | p.R213X |
| STAD | TCGA-D7-6525-01 | exon_skip_286379 | 7578177 | 7578289 | 7578212 | 7578212 | Nonsense_Mutation | G | A | p.R213* |
| STAD | TCGA-D7-6525-01 | exon_skip_286379 | 7578177 | 7578289 | 7578212 | 7578212 | Nonsense_Mutation | G | A | p.R213X |
| UCEC | TCGA-BS-A0UF-01 | exon_skip_286379 | 7578177 | 7578289 | 7578212 | 7578212 | Nonsense_Mutation | G | A | p.R213* |
| UCEC | TCGA-BS-A0UV-01 | exon_skip_286379 | 7578177 | 7578289 | 7578212 | 7578212 | Nonsense_Mutation | G | A | p.R213* |
| UCS | TCGA-ND-A4WC-01 | exon_skip_286379 | 7578177 | 7578289 | 7578212 | 7578212 | Nonsense_Mutation | G | A | p.R213* |
| UCS | TCGA-ND-A4WC-01 | exon_skip_286379 | 7578177 | 7578289 | 7578212 | 7578212 | Nonsense_Mutation | G | A | p.R213X |
| LUAD | TCGA-50-5045-01 | exon_skip_286379 | 7578177 | 7578289 | 7578224 | 7578224 | Nonsense_Mutation | T | A | p.R209* |
| HNSC | TCGA-P3-A6T4-01 | exon_skip_286379 | 7578177 | 7578289 | 7578234 | 7578234 | Nonsense_Mutation | A | T | p.Y205* |
| BLCA | TCGA-BT-A20X-01 | exon_skip_286379 | 7578177 | 7578289 | 7578239 | 7578239 | Nonsense_Mutation | C | A | p.E204* |
| BLCA | TCGA-XF-A9SK-01 | exon_skip_286379 | 7578177 | 7578289 | 7578239 | 7578239 | Nonsense_Mutation | C | A | p.E204* |
| ESCA | TCGA-LN-A9FO-01 | exon_skip_286379 | 7578177 | 7578289 | 7578239 | 7578239 | Nonsense_Mutation | C | A | p.E204* |
| ESCA | TCGA-LN-A9FO-01 | exon_skip_286379 | 7578177 | 7578289 | 7578239 | 7578239 | Nonsense_Mutation | C | A | p.E204X |
| HNSC | TCGA-QK-A8Z7-01 | exon_skip_286379 | 7578177 | 7578289 | 7578239 | 7578239 | Nonsense_Mutation | C | A | p.E204* |
| LIHC | TCGA-WJ-A86L-01 | exon_skip_286379 | 7578177 | 7578289 | 7578239 | 7578239 | Nonsense_Mutation | C | A | p.E204X |
| LUSC | TCGA-60-2721-01 | exon_skip_286379 | 7578177 | 7578289 | 7578239 | 7578239 | Nonsense_Mutation | C | A | p.E204* |
| OV | TCGA-61-2002-01 | exon_skip_286379 | 7578177 | 7578289 | 7578239 | 7578239 | Nonsense_Mutation | C | A | p.E204* |
| OV | TCGA-61-2016-01 | exon_skip_286379 | 7578177 | 7578289 | 7578239 | 7578239 | Nonsense_Mutation | C | A | p.E204* |
| HNSC | TCGA-BA-5557-01 | exon_skip_286379 | 7578177 | 7578289 | 7578247 | 7578247 | Nonsense_Mutation | A | T | p.L201* |
| HNSC | TCGA-CN-5359-01 | exon_skip_286379 | 7578177 | 7578289 | 7578247 | 7578247 | Nonsense_Mutation | A | T | p.L201* |
| HNSC | TCGA-UF-A7JF-01 | exon_skip_286379 | 7578177 | 7578289 | 7578254 | 7578254 | Nonsense_Mutation | C | A | p.G199* |
| PAAD | TCGA-IB-7890-01 | exon_skip_286379 | 7578177 | 7578289 | 7578254 | 7578254 | Nonsense_Mutation | C | A | p.G199* |
| PAAD | TCGA-IB-7890-01 | exon_skip_286379 | 7578177 | 7578289 | 7578254 | 7578254 | Nonsense_Mutation | C | A | p.G199X |
| BRCA | TCGA-AR-A0TS-01 | exon_skip_286379 | 7578177 | 7578289 | 7578257 | 7578257 | Nonsense_Mutation | C | A | p.E198* |
| COAD | TCGA-A6-2675-01 | exon_skip_286379 | 7578177 | 7578289 | 7578257 | 7578257 | Nonsense_Mutation | C | A | p.E198X |
| ESCA | TCGA-JY-A6FA-01 | exon_skip_286379 | 7578177 | 7578289 | 7578257 | 7578257 | Nonsense_Mutation | C | A | p.E198* |
| ESCA | TCGA-JY-A6FA-01 | exon_skip_286379 | 7578177 | 7578289 | 7578257 | 7578257 | Nonsense_Mutation | C | A | p.E198X |
| ESCA | TCGA-L5-A4OJ-01 | exon_skip_286379 | 7578177 | 7578289 | 7578257 | 7578257 | Nonsense_Mutation | C | A | p.E198* |
| ESCA | TCGA-L5-A4OJ-01 | exon_skip_286379 | 7578177 | 7578289 | 7578257 | 7578257 | Nonsense_Mutation | C | A | p.E198X |
| LUAD | TCGA-17-Z023-01 | exon_skip_286379 | 7578177 | 7578289 | 7578257 | 7578257 | Nonsense_Mutation | C | A | p.E198* |
| LUAD | TCGA-62-A46R-01 | exon_skip_286379 | 7578177 | 7578289 | 7578257 | 7578257 | Nonsense_Mutation | C | A | p.E198* |
| LUAD | TCGA-NJ-A4YF-01 | exon_skip_286379 | 7578177 | 7578289 | 7578257 | 7578257 | Nonsense_Mutation | C | A | p.E198* |
| OV | TCGA-24-1413-01 | exon_skip_286379 | 7578177 | 7578289 | 7578257 | 7578257 | Nonsense_Mutation | C | A | p.E198* |
| SKCM | TCGA-EE-A29V-06 | exon_skip_286379 | 7578177 | 7578289 | 7578257 | 7578257 | Nonsense_Mutation | C | A | p.E198X |
| STAD | TCGA-R5-A7ZF-01 | exon_skip_286379 | 7578177 | 7578289 | 7578257 | 7578257 | Nonsense_Mutation | C | A | p.E198* |
| STAD | TCGA-R5-A7ZF-01 | exon_skip_286379 | 7578177 | 7578289 | 7578257 | 7578257 | Nonsense_Mutation | C | A | p.E198X |
| BRCA | TCGA-A2-A0CW-01 | exon_skip_286379 | 7578177 | 7578289 | 7578263 | 7578263 | Nonsense_Mutation | G | A | p.R196* |
| BRCA | TCGA-A2-A0D0-01 | exon_skip_286379 | 7578177 | 7578289 | 7578263 | 7578263 | Nonsense_Mutation | G | A | p.R196* |
| BRCA | TCGA-AR-A1AP-01 | exon_skip_286379 | 7578177 | 7578289 | 7578263 | 7578263 | Nonsense_Mutation | G | A | p.R196* |
| BRCA | TCGA-B6-A0RU-01 | exon_skip_286379 | 7578177 | 7578289 | 7578263 | 7578263 | Nonsense_Mutation | G | A | p.R196* |
| BRCA | TCGA-C8-A1HJ-01 | exon_skip_286379 | 7578177 | 7578289 | 7578263 | 7578263 | Nonsense_Mutation | G | A | p.R196* |
| BRCA | TCGA-D8-A27M-01 | exon_skip_286379 | 7578177 | 7578289 | 7578263 | 7578263 | Nonsense_Mutation | G | A | p.R196* |
| BRCA | TCGA-E2-A14N-01 | exon_skip_286379 | 7578177 | 7578289 | 7578263 | 7578263 | Nonsense_Mutation | G | A | p.R196* |
| BRCA | TCGA-E9-A1N9-01 | exon_skip_286379 | 7578177 | 7578289 | 7578263 | 7578263 | Nonsense_Mutation | G | A | p.R196* |
| COAD | TCGA-AA-A00D-01 | exon_skip_286379 | 7578177 | 7578289 | 7578263 | 7578263 | Nonsense_Mutation | G | A | p.R196X |
| COAD | TCGA-G4-6299-01 | exon_skip_286379 | 7578177 | 7578289 | 7578263 | 7578263 | Nonsense_Mutation | G | A | p.R196X |
| ESCA | TCGA-2H-A9GK-01 | exon_skip_286379 | 7578177 | 7578289 | 7578263 | 7578263 | Nonsense_Mutation | G | A | p.R196* |
| ESCA | TCGA-2H-A9GK-01 | exon_skip_286379 | 7578177 | 7578289 | 7578263 | 7578263 | Nonsense_Mutation | G | A | p.R196X |
| ESCA | TCGA-JY-A6F8-01 | exon_skip_286379 | 7578177 | 7578289 | 7578263 | 7578263 | Nonsense_Mutation | G | A | p.R196* |
| ESCA | TCGA-JY-A6F8-01 | exon_skip_286379 | 7578177 | 7578289 | 7578263 | 7578263 | Nonsense_Mutation | G | A | p.R196X |
| ESCA | TCGA-L5-A8NV-01 | exon_skip_286379 | 7578177 | 7578289 | 7578263 | 7578263 | Nonsense_Mutation | G | A | p.R196* |
| ESCA | TCGA-L5-A8NV-01 | exon_skip_286379 | 7578177 | 7578289 | 7578263 | 7578263 | Nonsense_Mutation | G | A | p.R196X |
| GBM | TCGA-06-2567-01 | exon_skip_286379 | 7578177 | 7578289 | 7578263 | 7578263 | Nonsense_Mutation | G | A | p.R196* |
| GBM | TCGA-06-5417-01 | exon_skip_286379 | 7578177 | 7578289 | 7578263 | 7578263 | Nonsense_Mutation | G | A | p.R196* |
| GBM | TCGA-14-1825-01 | exon_skip_286379 | 7578177 | 7578289 | 7578263 | 7578263 | Nonsense_Mutation | G | A | p.R196* |
| HNSC | TCGA-BA-A6DG-01 | exon_skip_286379 | 7578177 | 7578289 | 7578263 | 7578263 | Nonsense_Mutation | G | A | p.R196* |
| HNSC | TCGA-CQ-A4CE-01 | exon_skip_286379 | 7578177 | 7578289 | 7578263 | 7578263 | Nonsense_Mutation | G | A | p.R196* |
| HNSC | TCGA-CR-6484-01 | exon_skip_286379 | 7578177 | 7578289 | 7578263 | 7578263 | Nonsense_Mutation | G | A | p.R196* |
| HNSC | TCGA-CV-7095-01 | exon_skip_286379 | 7578177 | 7578289 | 7578263 | 7578263 | Nonsense_Mutation | G | A | p.R196* |
| HNSC | TCGA-CV-7238-01 | exon_skip_286379 | 7578177 | 7578289 | 7578263 | 7578263 | Nonsense_Mutation | G | A | p.R196* |
| HNSC | TCGA-H7-A6C4-01 | exon_skip_286379 | 7578177 | 7578289 | 7578263 | 7578263 | Nonsense_Mutation | G | A | p.R196* |
| HNSC | TCGA-IQ-A61H-01 | exon_skip_286379 | 7578177 | 7578289 | 7578263 | 7578263 | Nonsense_Mutation | G | A | p.R196* |
| KICH | TCGA-KN-8428-01 | exon_skip_286379 | 7578177 | 7578289 | 7578263 | 7578263 | Nonsense_Mutation | G | A | p.R196* |
| KICH | TCGA-KN-8428-01 | exon_skip_286379 | 7578177 | 7578289 | 7578263 | 7578263 | Nonsense_Mutation | G | A | p.R196X |
| LGG | TCGA-FG-6690-01 | exon_skip_286379 | 7578177 | 7578289 | 7578263 | 7578263 | Nonsense_Mutation | G | A | p.R196* |
| LGG | TCGA-FG-6690-01 | exon_skip_286379 | 7578177 | 7578289 | 7578263 | 7578263 | Nonsense_Mutation | G | A | p.R196X |
| LGG | TCGA-HT-7604-01 | exon_skip_286379 | 7578177 | 7578289 | 7578263 | 7578263 | Nonsense_Mutation | G | A | p.R196* |
| LGG | TCGA-HT-7604-01 | exon_skip_286379 | 7578177 | 7578289 | 7578263 | 7578263 | Nonsense_Mutation | G | A | p.R196X |
| LGG | TCGA-HW-8319-01 | exon_skip_286379 | 7578177 | 7578289 | 7578263 | 7578263 | Nonsense_Mutation | G | A | p.R196* |
| LGG | TCGA-HW-8319-01 | exon_skip_286379 | 7578177 | 7578289 | 7578263 | 7578263 | Nonsense_Mutation | G | A | p.R196X |
| LGG | TCGA-TQ-A8XE-01 | exon_skip_286379 | 7578177 | 7578289 | 7578263 | 7578263 | Nonsense_Mutation | G | A | p.R196* |
| LGG | TCGA-TQ-A8XE-02 | exon_skip_286379 | 7578177 | 7578289 | 7578263 | 7578263 | Nonsense_Mutation | G | A | p.R196* |
| LUAD | TCGA-05-4433-01 | exon_skip_286379 | 7578177 | 7578289 | 7578263 | 7578263 | Nonsense_Mutation | G | A | p.R196* |
| LUAD | TCGA-44-2666-01 | exon_skip_286379 | 7578177 | 7578289 | 7578263 | 7578263 | Nonsense_Mutation | G | A | p.R196* |
| LUAD | TCGA-73-7499-01 | exon_skip_286379 | 7578177 | 7578289 | 7578263 | 7578263 | Nonsense_Mutation | G | A | p.R196* |
| LUSC | TCGA-22-4604-01 | exon_skip_286379 | 7578177 | 7578289 | 7578263 | 7578263 | Nonsense_Mutation | G | A | p.R196* |
| OV | TCGA-13-0916-01 | exon_skip_286379 | 7578177 | 7578289 | 7578263 | 7578263 | Nonsense_Mutation | G | A | p.R196* |
| OV | TCGA-13-1405-01 | exon_skip_286379 | 7578177 | 7578289 | 7578263 | 7578263 | Nonsense_Mutation | G | A | p.R196* |
| OV | TCGA-24-2289-01 | exon_skip_286379 | 7578177 | 7578289 | 7578263 | 7578263 | Nonsense_Mutation | G | A | p.R196* |
| PAAD | TCGA-HZ-7922-01 | exon_skip_286379 | 7578177 | 7578289 | 7578263 | 7578263 | Nonsense_Mutation | G | A | p.R196* |
| PAAD | TCGA-HZ-7922-01 | exon_skip_286379 | 7578177 | 7578289 | 7578263 | 7578263 | Nonsense_Mutation | G | A | p.R196X |
| PAAD | TCGA-IB-7645-01 | exon_skip_286379 | 7578177 | 7578289 | 7578263 | 7578263 | Nonsense_Mutation | G | A | p.R196* |
| PAAD | TCGA-IB-7645-01 | exon_skip_286379 | 7578177 | 7578289 | 7578263 | 7578263 | Nonsense_Mutation | G | A | p.R196X |
| PAAD | TCGA-IB-A5SO-01 | exon_skip_286379 | 7578177 | 7578289 | 7578263 | 7578263 | Nonsense_Mutation | G | A | p.R196* |
| PAAD | TCGA-IB-A5SO-01 | exon_skip_286379 | 7578177 | 7578289 | 7578263 | 7578263 | Nonsense_Mutation | G | A | p.R196X |
| READ | TCGA-DC-6154-01 | exon_skip_286379 | 7578177 | 7578289 | 7578263 | 7578263 | Nonsense_Mutation | G | A | p.R196X |
| READ | TCGA-F5-6571-01 | exon_skip_286379 | 7578177 | 7578289 | 7578263 | 7578263 | Nonsense_Mutation | G | A | p.R196X |
| SKCM | TCGA-BF-A3DL-01 | exon_skip_286379 | 7578177 | 7578289 | 7578263 | 7578263 | Nonsense_Mutation | G | A | p.R196* |
| SKCM | TCGA-BF-A3DL-01 | exon_skip_286379 | 7578177 | 7578289 | 7578263 | 7578263 | Nonsense_Mutation | G | A | p.R196X |
| SKCM | TCGA-D3-A51G-06 | exon_skip_286379 | 7578177 | 7578289 | 7578263 | 7578263 | Nonsense_Mutation | G | A | p.R196* |
| SKCM | TCGA-D3-A51G-06 | exon_skip_286379 | 7578177 | 7578289 | 7578263 | 7578263 | Nonsense_Mutation | G | A | p.R196X |
| SKCM | TCGA-DA-A1I5-06 | exon_skip_286379 | 7578177 | 7578289 | 7578263 | 7578263 | Nonsense_Mutation | G | A | p.R196* |
| SKCM | TCGA-W3-AA1V-06 | exon_skip_286379 | 7578177 | 7578289 | 7578263 | 7578263 | Nonsense_Mutation | G | A | p.R196* |
| STAD | TCGA-BR-4363-01 | exon_skip_286379 | 7578177 | 7578289 | 7578263 | 7578263 | Nonsense_Mutation | G | A | p.R196* |
| STAD | TCGA-BR-4363-01 | exon_skip_286379 | 7578177 | 7578289 | 7578263 | 7578263 | Nonsense_Mutation | G | A | p.R196X |
| STAD | TCGA-VQ-A8DT-01 | exon_skip_286379 | 7578177 | 7578289 | 7578263 | 7578263 | Nonsense_Mutation | G | A | p.R196* |
| STAD | TCGA-VQ-A8DT-01 | exon_skip_286379 | 7578177 | 7578289 | 7578263 | 7578263 | Nonsense_Mutation | G | A | p.R196X |
| STAD | TCGA-VQ-A8PE-01 | exon_skip_286379 | 7578177 | 7578289 | 7578263 | 7578263 | Nonsense_Mutation | G | A | p.R196* |
| STAD | TCGA-VQ-A8PE-01 | exon_skip_286379 | 7578177 | 7578289 | 7578263 | 7578263 | Nonsense_Mutation | G | A | p.R196X |
| BLCA | TCGA-DK-A1A3-01 | exon_skip_286379 | 7578177 | 7578289 | 7578275 | 7578275 | Nonsense_Mutation | G | A | p.Q192* |
| BLCA | TCGA-DK-A2I1-01 | exon_skip_286379 | 7578177 | 7578289 | 7578275 | 7578275 | Nonsense_Mutation | G | A | p.Q192* |
| BLCA | TCGA-FD-A3NA-01 | exon_skip_286379 | 7578177 | 7578289 | 7578275 | 7578275 | Nonsense_Mutation | G | A | p.Q192* |
| BLCA | TCGA-GV-A3JZ-01 | exon_skip_286379 | 7578177 | 7578289 | 7578275 | 7578275 | Nonsense_Mutation | G | A | p.Q192* |
| BRCA | TCGA-EW-A1OY-01 | exon_skip_286379 | 7578177 | 7578289 | 7578275 | 7578275 | Nonsense_Mutation | G | A | p.Q192* |
| HNSC | TCGA-CV-6933-01 | exon_skip_286379 | 7578177 | 7578289 | 7578275 | 7578275 | Nonsense_Mutation | G | A | p.Q192* |
| HNSC | TCGA-IQ-A6SH-01 | exon_skip_286379 | 7578177 | 7578289 | 7578275 | 7578275 | Nonsense_Mutation | G | A | p.Q192* |
| HNSC | TCGA-RS-A6TO-01 | exon_skip_286379 | 7578177 | 7578289 | 7578275 | 7578275 | Nonsense_Mutation | G | A | p.Q192* |
| LIHC | TCGA-BW-A5NQ-01 | exon_skip_286379 | 7578177 | 7578289 | 7578275 | 7578275 | Nonsense_Mutation | G | A | p.Q192* |
| LIHC | TCGA-BW-A5NQ-01 | exon_skip_286379 | 7578177 | 7578289 | 7578275 | 7578275 | Nonsense_Mutation | G | A | p.Q192X |
| LIHC | TCGA-DD-AACG-01 | exon_skip_286379 | 7578177 | 7578289 | 7578275 | 7578275 | Nonsense_Mutation | G | A | p.Q192X |
| LUAD | TCGA-75-6207-01 | exon_skip_286379 | 7578177 | 7578289 | 7578275 | 7578275 | Nonsense_Mutation | G | A | p.Q192* |
| LUAD | TCGA-78-7535-01 | exon_skip_286379 | 7578177 | 7578289 | 7578275 | 7578275 | Nonsense_Mutation | G | A | p.Q192* |
| LUAD | TCGA-86-8073-01 | exon_skip_286379 | 7578177 | 7578289 | 7578275 | 7578275 | Nonsense_Mutation | G | A | p.Q192* |
| OV | TCGA-24-1474-01 | exon_skip_286379 | 7578177 | 7578289 | 7578275 | 7578275 | Nonsense_Mutation | G | A | p.Q192* |
| PAAD | TCGA-IB-7888-01 | exon_skip_286379 | 7578177 | 7578289 | 7578275 | 7578275 | Nonsense_Mutation | G | A | p.Q192* |
| PAAD | TCGA-IB-7888-01 | exon_skip_286379 | 7578177 | 7578289 | 7578275 | 7578275 | Nonsense_Mutation | G | A | p.Q192X |
| STAD | TCGA-D7-A4YU-01 | exon_skip_286379 | 7578177 | 7578289 | 7578275 | 7578275 | Nonsense_Mutation | G | A | p.Q192* |
| STAD | TCGA-D7-A4YU-01 | exon_skip_286379 | 7578177 | 7578289 | 7578275 | 7578275 | Nonsense_Mutation | G | A | p.Q192X |
| THCA | TCGA-EM-A1YB-01 | exon_skip_286379 | 7578177 | 7578289 | 7578275 | 7578275 | Nonsense_Mutation | G | A | p.Q192* |
| THCA | TCGA-EM-A1YB-01 | exon_skip_286379 | 7578177 | 7578289 | 7578275 | 7578275 | Nonsense_Mutation | G | A | p.Q192X |
| BRCA | TCGA-AR-A254-01 | exon_skip_286384 | 7579312 | 7579590 | 7579315 | 7579315 | Nonsense_Mutation | G | T | p.C124* |
| ESCA | TCGA-LN-A49U-01 | exon_skip_286384 | 7579312 | 7579590 | 7579315 | 7579315 | Nonsense_Mutation | G | T | p.C124* |
| ESCA | TCGA-LN-A49U-01 | exon_skip_286384 | 7579312 | 7579590 | 7579315 | 7579315 | Nonsense_Mutation | G | T | p.C124X |
| BRCA | TCGA-B6-A0WX-01 | exon_skip_286384 | 7579312 | 7579590 | 7579346 | 7579346 | Nonsense_Mutation | A | T | p.L114* |
| HNSC | TCGA-CV-7422-01 | exon_skip_286384 | 7579312 | 7579590 | 7579377 | 7579377 | Nonsense_Mutation | G | A | p.Q104* |
| LUAD | TCGA-17-Z062-01 | exon_skip_286384 | 7579312 | 7579590 | 7579377 | 7579377 | Nonsense_Mutation | G | A | p.Q104* |
| PAAD | TCGA-2J-AAB9-01 | exon_skip_286384 | 7579312 | 7579590 | 7579377 | 7579377 | Nonsense_Mutation | G | A | p.Q104* |
| PAAD | TCGA-2J-AAB9-01 | exon_skip_286384 | 7579312 | 7579590 | 7579377 | 7579377 | Nonsense_Mutation | G | A | p.Q104X |
| HNSC | TCGA-CV-7263-01 | exon_skip_286384 | 7579312 | 7579590 | 7579378 | 7579378 | Nonsense_Mutation | G | C | p.Y103* |
| HNSC | TCGA-H7-8502-01 | exon_skip_286384 | 7579312 | 7579590 | 7579378 | 7579378 | Nonsense_Mutation | G | T | p.Y103* |
| LUSC | TCGA-39-5031-01 | exon_skip_286384 | 7579312 | 7579590 | 7579378 | 7579378 | Nonsense_Mutation | G | T | p.Y103* |
| HNSC | TCGA-CQ-6228-01 | exon_skip_286384 | 7579312 | 7579590 | 7579386 | 7579386 | Nonsense_Mutation | T | A | p.K101* |
| COAD | TCGA-CM-6172-01 | exon_skip_286384 | 7579312 | 7579590 | 7579389 | 7579389 | Nonsense_Mutation | G | A | p.Q100X |
| OV | TCGA-13-0920-01 | exon_skip_286384 | 7579312 | 7579590 | 7579389 | 7579389 | Nonsense_Mutation | G | A | p.Q100* |
| UCS | TCGA-N8-A56S-01 | exon_skip_286384 | 7579312 | 7579590 | 7579389 | 7579389 | Nonsense_Mutation | G | A | p.Q100* |
| UCS | TCGA-N8-A56S-01 | exon_skip_286384 | 7579312 | 7579590 | 7579389 | 7579389 | Nonsense_Mutation | G | A | p.Q100X |
| BLCA | TCGA-ZF-AA53-01 | exon_skip_286384 | 7579312 | 7579590 | 7579406 | 7579406 | Nonsense_Mutation | G | C | p.S94* |
| COAD | TCGA-CA-6718-01 | exon_skip_286384 | 7579312 | 7579590 | 7579406 | 7579406 | Nonsense_Mutation | G | T | p.S94X |
| ESCA | TCGA-VR-AA4G-01 | exon_skip_286384 | 7579312 | 7579590 | 7579406 | 7579406 | Nonsense_Mutation | G | T | p.S94* |
| ESCA | TCGA-VR-AA4G-01 | exon_skip_286384 | 7579312 | 7579590 | 7579406 | 7579406 | Nonsense_Mutation | G | T | p.S94X |
| LGG | TCGA-DB-A4XC-01 | exon_skip_286384 | 7579312 | 7579590 | 7579406 | 7579406 | Nonsense_Mutation | G | C | p.S94* |
| LGG | TCGA-DB-A4XC-01 | exon_skip_286384 | 7579312 | 7579590 | 7579406 | 7579406 | Nonsense_Mutation | G | C | p.S94X |
| STAD | TCGA-BR-8678-01 | exon_skip_286384 | 7579312 | 7579590 | 7579406 | 7579406 | Nonsense_Mutation | G | C | p.S94* |
| STAD | TCGA-BR-8678-01 | exon_skip_286384 | 7579312 | 7579590 | 7579406 | 7579406 | Nonsense_Mutation | G | C | p.S94X |
| BRCA | TCGA-E9-A243-01 | exon_skip_286384 | 7579312 | 7579590 | 7579414 | 7579414 | Nonsense_Mutation | C | T | p.W91* |
| ESCA | TCGA-L5-A4OG-01 | exon_skip_286384 | 7579312 | 7579590 | 7579414 | 7579414 | Nonsense_Mutation | C | T | p.W91* |
| ESCA | TCGA-L5-A4OG-01 | exon_skip_286384 | 7579312 | 7579590 | 7579414 | 7579414 | Nonsense_Mutation | C | T | p.W91X |
| ESCA | TCGA-R6-A8WC-01 | exon_skip_286384 | 7579312 | 7579590 | 7579414 | 7579414 | Nonsense_Mutation | C | T | p.W91* |
| ESCA | TCGA-R6-A8WC-01 | exon_skip_286384 | 7579312 | 7579590 | 7579414 | 7579414 | Nonsense_Mutation | C | T | p.W91X |
| LUAD | TCGA-50-5931-01 | exon_skip_286384 | 7579312 | 7579590 | 7579414 | 7579414 | Nonsense_Mutation | C | T | p.W91* |
| LUSC | TCGA-21-5784-01 | exon_skip_286384 | 7579312 | 7579590 | 7579414 | 7579414 | Nonsense_Mutation | C | T | p.W91* |
| SARC | TCGA-3B-A9HT-01 | exon_skip_286384 | 7579312 | 7579590 | 7579414 | 7579414 | Nonsense_Mutation | C | T | p.W91* |
| STAD | TCGA-BR-A4PD-01 | exon_skip_286384 | 7579312 | 7579590 | 7579414 | 7579414 | Nonsense_Mutation | C | T | p.W91* |
| STAD | TCGA-BR-A4PD-01 | exon_skip_286384 | 7579312 | 7579590 | 7579414 | 7579414 | Nonsense_Mutation | C | T | p.W91X |
| BLCA | TCGA-XF-A8HH-01 | exon_skip_286384 | 7579312 | 7579590 | 7579415 | 7579415 | Nonsense_Mutation | C | T | p.W91* |
| COAD | TCGA-CM-5860-01 | exon_skip_286384 | 7579312 | 7579590 | 7579415 | 7579415 | Nonsense_Mutation | C | T | p.W91X |
| HNSC | TCGA-CV-5435-01 | exon_skip_286384 | 7579312 | 7579590 | 7579415 | 7579415 | Nonsense_Mutation | C | T | p.W91* |
| KIRP | TCGA-B3-4104-01 | exon_skip_286384 | 7579312 | 7579590 | 7579415 | 7579415 | Nonsense_Mutation | C | T | p.W91* |
| KIRP | TCGA-B3-4104-01 | exon_skip_286384 | 7579312 | 7579590 | 7579415 | 7579415 | Nonsense_Mutation | C | T | p.W91X |
| LGG | TCGA-S9-A6WO-01 | exon_skip_286384 | 7579312 | 7579590 | 7579415 | 7579415 | Nonsense_Mutation | C | T | p.W91* |
| SARC | TCGA-HB-A5W3-01 | exon_skip_286384 | 7579312 | 7579590 | 7579415 | 7579415 | Nonsense_Mutation | C | T | p.W91* |
| BLCA | TCGA-ZF-AA4X-01 | exon_skip_286384 | 7579312 | 7579590 | 7579485 | 7579485 | Nonsense_Mutation | C | A | p.E68* |
| HNSC | TCGA-D6-A74Q-01 | exon_skip_286384 | 7579312 | 7579590 | 7579485 | 7579485 | Nonsense_Mutation | C | A | p.E68* |
| HNSC | TCGA-UF-A7JA-01 | exon_skip_286384 | 7579312 | 7579590 | 7579485 | 7579485 | Nonsense_Mutation | C | A | p.E68* |
| LUAD | TCGA-05-5425-01 | exon_skip_286384 | 7579312 | 7579590 | 7579485 | 7579485 | Nonsense_Mutation | C | A | p.E68* |
| LUAD | TCGA-44-7662-01 | exon_skip_286384 | 7579312 | 7579590 | 7579485 | 7579485 | Nonsense_Mutation | C | A | p.E68* |
| LUSC | TCGA-37-4135-01 | exon_skip_286384 | 7579312 | 7579590 | 7579485 | 7579485 | Nonsense_Mutation | C | A | p.E68* |
| LUAD | TCGA-17-Z061-01 | exon_skip_286384 | 7579312 | 7579590 | 7579494 | 7579494 | Nonsense_Mutation | T | A | p.R65* |
| LUSC | TCGA-37-3789-01 | exon_skip_286384 | 7579312 | 7579590 | 7579494 | 7579494 | Nonsense_Mutation | T | A | p.R65* |
| ACC | TCGA-OR-A5JA-01 | exon_skip_286384 | 7579312 | 7579590 | 7579521 | 7579521 | Nonsense_Mutation | C | A | p.E56X |
| BRCA | TCGA-BH-A18V-01 | exon_skip_286384 | 7579312 | 7579590 | 7579521 | 7579521 | Nonsense_Mutation | C | A | p.E56* |
| HNSC | TCGA-CV-5436-01 | exon_skip_286384 | 7579312 | 7579590 | 7579521 | 7579521 | Nonsense_Mutation | C | A | p.E56* |
| HNSC | TCGA-H7-8501-01 | exon_skip_286384 | 7579312 | 7579590 | 7579521 | 7579521 | Nonsense_Mutation | C | A | p.E56* |
| SARC | TCGA-HS-A5N9-01 | exon_skip_286384 | 7579312 | 7579590 | 7579521 | 7579521 | Nonsense_Mutation | C | A | p.E56* |
| LUAD | TCGA-44-A4SU-01 | exon_skip_286384 | 7579312 | 7579590 | 7579528 | 7579528 | Nonsense_Mutation | C | T | p.W53* |
| BLCA | TCGA-FD-A3SO-01 | exon_skip_286384 | 7579312 | 7579590 | 7579529 | 7579529 | Nonsense_Mutation | C | T | p.W53* |
| HNSC | TCGA-CV-7252-01 | exon_skip_286384 | 7579312 | 7579590 | 7579533 | 7579533 | Nonsense_Mutation | G | A | p.Q52* |
| LUAD | TCGA-55-7727-01 | exon_skip_286384 | 7579312 | 7579590 | 7579533 | 7579533 | Nonsense_Mutation | G | A | p.Q52* |
| ESCA | TCGA-R6-A8W8-01 | exon_skip_286384 | 7579312 | 7579590 | 7579536 | 7579536 | Nonsense_Mutation | C | A | p.E51* |
| ESCA | TCGA-R6-A8W8-01 | exon_skip_286384 | 7579312 | 7579590 | 7579536 | 7579536 | Nonsense_Mutation | C | A | p.E51X |
| READ | TCGA-G5-6235-01 | exon_skip_286384 | 7579312 | 7579590 | 7579536 | 7579536 | Nonsense_Mutation | C | A | p.E51X |
| HNSC | TCGA-CV-7104-01 | exon_skip_286384 | 7579312 | 7579590 | 7579575 | 7579575 | Nonsense_Mutation | G | A | p.Q38* |
| PAAD | TCGA-2L-AAQE-01 | exon_skip_286384 | 7579312 | 7579590 | 7579575 | 7579575 | Nonsense_Mutation | G | A | p.Q38* |
| PAAD | TCGA-2L-AAQE-01 | exon_skip_286384 | 7579312 | 7579590 | 7579575 | 7579575 | Nonsense_Mutation | G | A | p.Q38X |
| HNSC | TCGA-CN-6019-01 | exon_skip_286364 | 7573927 | 7574033 | 7574034 | 7574034 | Splice_Site | C | A | p.I332_splice |
| LGG | TCGA-DU-A5TW-01 | exon_skip_286364 | 7573927 | 7574033 | 7574034 | 7574034 | Splice_Site | C | G | . |
| OV | TCGA-13-1498-01 | exon_skip_286364 | 7573927 | 7574033 | 7574034 | 7574034 | Splice_Site | C | T | e9-1 |
| SARC | TCGA-SG-A6Z4-01 | exon_skip_286364 | 7573927 | 7574033 | 7574034 | 7574034 | Splice_Site | C | G | e9-1 |
| UCEC | TCGA-D1-A16I-01 | exon_skip_286364 | 7573927 | 7574033 | 7574034 | 7574034 | Splice_Site | C | G | e9-1 |
| UCEC | TCGA-D1-A16I-01 | exon_skip_286364 | 7573927 | 7574033 | 7574034 | 7574034 | Splice_Site | C | G | p.I332_splice |
| DLBC | TCGA-GR-A4D4-01 | exon_skip_286364 | 7573927 | 7574033 | 7574035 | 7574035 | Splice_Site | T | C | . |
| ESCA | TCGA-LN-A8HZ-01 | exon_skip_286364 | 7573927 | 7574033 | 7574035 | 7574035 | Splice_Site | T | G | . |
| ESCA | TCGA-LN-A8HZ-01 | exon_skip_286364 | 7573927 | 7574033 | 7574035 | 7574035 | Splice_Site | T | G | e9-2 |
| LGG | TCGA-DH-5140-01 | exon_skip_286364 | 7573927 | 7574033 | 7574035 | 7574035 | Splice_Site | T | G | . |
| LIHC | TCGA-G3-A5SM-01 | exon_skip_286364 | 7573927 | 7574033 | 7574035 | 7574035 | Splice_Site | T | C | . |
| LUSC | TCGA-66-2783-01 | exon_skip_286364 | 7573927 | 7574033 | 7574035 | 7574035 | Splice_Site | T | C | p.I332_splice |
| HNSC | TCGA-CV-7097-01 | exon_skip_286371 | 7576853 | 7576926 | 7576840 | 7576851 | Splice_Site | CAAGACTTAGTA | - | p.Q331_splice |
| BRCA | TCGA-D8-A143-01 | exon_skip_286371 | 7576853 | 7576926 | 7576851 | 7576851 | Splice_Site | A | C | e8+2 |
| LUSC | TCGA-66-2765-01 | exon_skip_286371 | 7576853 | 7576926 | 7576851 | 7576851 | Splice_Site | A | T | p.Q331_splice |
| BRCA | TCGA-B6-A0X1-01 | exon_skip_286371 | 7576853 | 7576926 | 7576852 | 7576852 | Splice_Site | C | A | e8+1 |
| BRCA | TCGA-D8-A1JK-01 | exon_skip_286371 | 7576853 | 7576926 | 7576852 | 7576852 | Splice_Site | C | T | e8+1 |
| COAD | TCGA-CA-6719-01 | exon_skip_286371 | 7576853 | 7576926 | 7576852 | 7576852 | Splice_Site | C | A | . |
| COAD | TCGA-CM-6165-01 | exon_skip_286371 | 7576853 | 7576926 | 7576852 | 7576852 | Splice_Site | C | A | . |
| COAD | TCGA-DM-A285-01 | exon_skip_286371 | 7576853 | 7576926 | 7576852 | 7576852 | Splice_Site | C | T | . |
| HNSC | TCGA-CR-7383-01 | exon_skip_286371 | 7576853 | 7576926 | 7576852 | 7576852 | Splice_Site | C | T | p.Q331_splice |
| OV | TCGA-23-2072-01 | exon_skip_286371 | 7576853 | 7576926 | 7576852 | 7576852 | Splice_Site | C | T | p.Q331_splice |
| OV | TCGA-24-1436-01 | exon_skip_286371 | 7576853 | 7576926 | 7576852 | 7576852 | Splice_Site | C | G | e8+1 |
| OV | TCGA-59-2355-01 | exon_skip_286371 | 7576853 | 7576926 | 7576852 | 7576852 | Splice_Site | C | A | p.Q331_splice |
| PAAD | TCGA-HZ-8005-01 | exon_skip_286371 | 7576853 | 7576926 | 7576852 | 7576852 | Splice_Site | C | T | . |
| SARC | TCGA-DX-A48V-01 | exon_skip_286371 | 7576853 | 7576926 | 7576852 | 7576852 | Splice_Site | C | A | e8+1 |
| GBM | TCGA-06-0188-01 | exon_skip_286371 | 7576853 | 7576926 | 7576926 | 7576927 | Splice_Site | GC | AT | p.A307_splice |
| HNSC | TCGA-CQ-5331-01 | exon_skip_286371 | 7576853 | 7576926 | 7576927 | 7576927 | Splice_Site | C | G | p.A307_splice |
| HNSC | TCGA-CV-6948-01 | exon_skip_286371 | 7576853 | 7576926 | 7576928 | 7576928 | Splice_Site | T | C | p.A307_splice |
| LIHC | TCGA-K7-A5RG-01 | exon_skip_286371 | 7576853 | 7576926 | 7576928 | 7576928 | Splice_Site | T | C | . |
| LIHC | TCGA-WX-AA44-01 | exon_skip_286371 | 7576853 | 7576926 | 7576928 | 7576928 | Splice_Site | T | C | . |
| LUSC | TCGA-39-5024-01 | exon_skip_286371 | 7576853 | 7576926 | 7576928 | 7576928 | Splice_Site | T | A | p.A307_splice |
| STAD | TCGA-HU-A4GC-01 | exon_skip_286371 | 7576853 | 7576926 | 7576928 | 7576928 | Splice_Site | T | - | . |
| STAD | TCGA-HU-A4GC-01 | exon_skip_286371 | 7576853 | 7576926 | 7576928 | 7576928 | Splice_Site | T | - | p.A307_splice |
| SARC | TCGA-MB-A5Y9-01 | exon_skip_286376 | 7577019 | 7577155 | 7577010 | 7577018 | Splice_Site | CTTGCTTAC | - | e7+1 |
| COAD | TCGA-DM-A1D0-01 | exon_skip_286376 | 7577019 | 7577155 | 7577017 | 7577017 | Splice_Site | A | C | . |
| ESCA | TCGA-R6-A6Y0-01 | exon_skip_286376 | 7577019 | 7577155 | 7577017 | 7577017 | Splice_Site | A | C | . |
| ESCA | TCGA-R6-A6Y0-01 | exon_skip_286376 | 7577019 | 7577155 | 7577017 | 7577017 | Splice_Site | A | C | e7+2 |
| ESCA | TCGA-V5-A7RE-01 | exon_skip_286376 | 7577019 | 7577155 | 7577017 | 7577017 | Splice_Site | A | C | . |
| ESCA | TCGA-V5-A7RE-01 | exon_skip_286376 | 7577019 | 7577155 | 7577017 | 7577017 | Splice_Site | A | C | e7+2 |
| ACC | TCGA-PK-A5HB-01 | exon_skip_286376 | 7577019 | 7577155 | 7577018 | 7577018 | Splice_Site | C | A | . |
| BRCA | TCGA-B6-A0IE-01 | exon_skip_286376 | 7577019 | 7577155 | 7577018 | 7577018 | Splice_Site | C | T | e7+1 |
| ESCA | TCGA-V5-A7RC-01 | exon_skip_286376 | 7577019 | 7577155 | 7577018 | 7577018 | Splice_Site | C | T | . |
| ESCA | TCGA-V5-A7RC-01 | exon_skip_286376 | 7577019 | 7577155 | 7577018 | 7577018 | Splice_Site | C | T | e7+1 |
| HNSC | TCGA-CV-5432-01 | exon_skip_286376 | 7577019 | 7577155 | 7577018 | 7577018 | Splice_Site | C | A | p.A307_splice |
| KICH | TCGA-KL-8335-01 | exon_skip_286376 | 7577019 | 7577155 | 7577018 | 7577018 | Splice_Site | C | T | . |
| KICH | TCGA-KL-8335-01 | exon_skip_286376 | 7577019 | 7577155 | 7577018 | 7577018 | Splice_Site | C | T | p.A307_splice |
| OV | TCGA-24-1103-01 | exon_skip_286376 | 7577019 | 7577155 | 7577018 | 7577018 | Splice_Site | C | T | e7+1 |
| OV | TCGA-23-1116-01 | exon_skip_286376 | 7577019 | 7577155 | 7577146 | 7577156 | Splice_Site | TAGATTACCAC | - | p.S261_splice |
| LUSC | TCGA-66-2767-01 | exon_skip_286376 | 7577019 | 7577155 | 7577156 | 7577156 | Splice_Site | C | A | p.S261_splice |
| STAD | TCGA-BR-7723-01 | exon_skip_286376 | 7577019 | 7577155 | 7577156 | 7577156 | Splice_Site | C | T | . |
| STAD | TCGA-BR-7723-01 | exon_skip_286376 | 7577019 | 7577155 | 7577156 | 7577156 | Splice_Site | C | T | p.S261_splice |
| LGG | TCGA-FG-A60J-01 | exon_skip_286376 | 7577019 | 7577155 | 7577157 | 7577157 | Splice_Site | T | G | . |
| BRCA | TCGA-A8-A09Q-01 | exon_skip_286379 | 7578177 | 7578289 | 7578175 | 7578175 | Splice_Site | A | T | e5+2 |
| ESCA | TCGA-IG-A625-01 | exon_skip_286379 | 7578177 | 7578289 | 7578176 | 7578176 | Splice_Site | C | A | . |
| ESCA | TCGA-IG-A625-01 | exon_skip_286379 | 7578177 | 7578289 | 7578176 | 7578176 | Splice_Site | C | A | e5+1 |
| KICH | TCGA-KO-8408-01 | exon_skip_286379 | 7578177 | 7578289 | 7578176 | 7578176 | Splice_Site | C | A | p.E224_splice |
| LGG | TCGA-HT-7609-01 | exon_skip_286379 | 7578177 | 7578289 | 7578176 | 7578176 | Splice_Site | C | T | . |
| LUSC | TCGA-60-2723-01 | exon_skip_286379 | 7578177 | 7578289 | 7578176 | 7578176 | Splice_Site | C | A | p.E224_splice |
| OV | TCGA-25-2400-01 | exon_skip_286379 | 7578177 | 7578289 | 7578176 | 7578176 | Splice_Site | C | A | p.E224_splice |
| SARC | TCGA-DX-AB2V-01 | exon_skip_286379 | 7578177 | 7578289 | 7578176 | 7578176 | Splice_Site | C | A | e5+1 |
| SARC | TCGA-WK-A8XY-01 | exon_skip_286379 | 7578177 | 7578289 | 7578176 | 7578176 | Splice_Site | C | A | e5+1 |
| SKCM | TCGA-ER-A19E-06 | exon_skip_286379 | 7578177 | 7578289 | 7578176 | 7578176 | Splice_Site | C | T | . |
| STAD | TCGA-B7-5818-01 | exon_skip_286379 | 7578177 | 7578289 | 7578176 | 7578176 | Splice_Site | C | T | . |
| STAD | TCGA-B7-5818-01 | exon_skip_286379 | 7578177 | 7578289 | 7578176 | 7578176 | Splice_Site | C | T | p.E224_splice |
| OV | TCGA-09-2044-01 | exon_skip_286379 | 7578177 | 7578289 | 7578266 | 7578290 | Splice_Site | TAAGATGCTGAGGAGGGGCCAGACC | - | p.G187_splice |
| BRCA | TCGA-BH-A0B7-01 | exon_skip_286379 | 7578177 | 7578289 | 7578290 | 7578290 | Splice_Site | C | T | e5-1 |
| BRCA | TCGA-BH-A208-01 | exon_skip_286379 | 7578177 | 7578289 | 7578290 | 7578290 | Splice_Site | C | G | e5-1 |
| ESCA | TCGA-LN-A9FR-01 | exon_skip_286379 | 7578177 | 7578289 | 7578290 | 7578290 | Splice_Site | C | G | . |
| ESCA | TCGA-LN-A9FR-01 | exon_skip_286379 | 7578177 | 7578289 | 7578290 | 7578290 | Splice_Site | C | G | e5-1 |
| LIHC | TCGA-T1-A6J8-01 | exon_skip_286379 | 7578177 | 7578289 | 7578290 | 7578290 | Splice_Site | C | T | . |
| LUAD | TCGA-50-5933-01 | exon_skip_286379 | 7578177 | 7578289 | 7578290 | 7578290 | Splice_Site | C | A | p.G187_splice |
| LUAD | TCGA-99-7458-01 | exon_skip_286379 | 7578177 | 7578289 | 7578290 | 7578290 | Splice_Site | C | T | p.G187_splice |
| OV | TCGA-10-0935-01 | exon_skip_286379 | 7578177 | 7578289 | 7578290 | 7578290 | Splice_Site | C | G | e5-1 |
| OV | TCGA-24-0970-01 | exon_skip_286379 | 7578177 | 7578289 | 7578290 | 7578290 | Splice_Site | C | T | p.G187_splice |
| SARC | TCGA-DX-A6BA-01 | exon_skip_286379 | 7578177 | 7578289 | 7578290 | 7578290 | Splice_Site | C | T | e5-1 |
| SARC | TCGA-DX-A8BK-01 | exon_skip_286379 | 7578177 | 7578289 | 7578290 | 7578290 | Splice_Site | C | G | e5-1 |
| UCS | TCGA-N6-A4VG-01 | exon_skip_286379 | 7578177 | 7578289 | 7578290 | 7578290 | Splice_Site | C | T | . |
| ESCA | TCGA-IG-A97H-01 | exon_skip_286379 | 7578177 | 7578289 | 7578291 | 7578291 | Splice_Site | T | A | . |
| ESCA | TCGA-IG-A97H-01 | exon_skip_286379 | 7578177 | 7578289 | 7578291 | 7578291 | Splice_Site | T | A | e5-2 |
| LGG | TCGA-HT-8114-01 | exon_skip_286379 | 7578177 | 7578289 | 7578291 | 7578291 | Splice_Site | T | C | . |
| SKCM | TCGA-D9-A6EC-06 | exon_skip_286379 | 7578177 | 7578289 | 7578291 | 7578291 | Splice_Site | T | G | . |
| UCS | TCGA-N5-A4R8-01 | exon_skip_286379 | 7578177 | 7578289 | 7578291 | 7578291 | Splice_Site | T | G | . |
| HNSC | TCGA-CN-4726-01 | exon_skip_286384 | 7579312 | 7579590 | 7579310 | 7579310 | Splice_Site | A | T | p.T125_splice |
| LUAD | TCGA-97-7938-01 | exon_skip_286384 | 7579312 | 7579590 | 7579310 | 7579310 | Splice_Site | A | T | p.T125_splice |
| SKCM | TCGA-EE-A2MQ-06 | exon_skip_286384 | 7579312 | 7579590 | 7579310 | 7579310 | Splice_Site | A | G | . |
| ACC | TCGA-OR-A5JG-01 | exon_skip_286384 | 7579312 | 7579590 | 7579311 | 7579311 | Splice_Site | C | A | . |
| BRCA | TCGA-A2-A0YG-01 | exon_skip_286384 | 7579312 | 7579590 | 7579311 | 7579311 | Splice_Site | C | A | e3+1 |
| BRCA | TCGA-A8-A07O-01 | exon_skip_286384 | 7579312 | 7579590 | 7579311 | 7579311 | Splice_Site | C | T | e3+1 |
| LGG | TCGA-DU-7007-01 | exon_skip_286384 | 7579312 | 7579590 | 7579311 | 7579311 | Splice_Site | C | G | . |
| LGG | TCGA-DU-7304-01 | exon_skip_286384 | 7579312 | 7579590 | 7579311 | 7579311 | Splice_Site | C | - | . |
| LGG | TCGA-FG-8182-01 | exon_skip_286384 | 7579312 | 7579590 | 7579311 | 7579311 | Splice_Site | C | T | . |
| LUSC | TCGA-34-5239-01 | exon_skip_286384 | 7579312 | 7579590 | 7579311 | 7579311 | Splice_Site | C | A | p.T125_splice |
| LUSC | TCGA-66-2788-01 | exon_skip_286384 | 7579312 | 7579590 | 7579311 | 7579311 | Splice_Site | C | A | p.T125_splice |
| OV | TCGA-13-1403-01 | exon_skip_286384 | 7579312 | 7579590 | 7579311 | 7579311 | Splice_Site | C | A | e3+1 |
| PAAD | TCGA-IB-7649-01 | exon_skip_286384 | 7579312 | 7579590 | 7579311 | 7579311 | Splice_Site | C | T | . |
| SARC | TCGA-LI-A9QH-01 | exon_skip_286384 | 7579312 | 7579590 | 7579311 | 7579311 | Splice_Site | C | T | e3+1 |
| STAD | TCGA-BR-8369-01 | exon_skip_286384 | 7579312 | 7579590 | 7579311 | 7579311 | Splice_Site | C | T | . |
| STAD | TCGA-BR-8369-01 | exon_skip_286384 | 7579312 | 7579590 | 7579311 | 7579311 | Splice_Site | C | T | p.T125_splice |
| STAD | TCGA-BR-8483-01 | exon_skip_286384 | 7579312 | 7579590 | 7579311 | 7579311 | Splice_Site | C | T | . |
| STAD | TCGA-BR-8483-01 | exon_skip_286384 | 7579312 | 7579590 | 7579311 | 7579311 | Splice_Site | C | T | p.T125_splice |
| BRCA | TCGA-E2-A155-01 | exon_skip_286384 | 7579312 | 7579590 | 7579591 | 7579591 | Splice_Site | C | G | e3-1 |
| HNSC | TCGA-CN-4740-01 | exon_skip_286384 | 7579312 | 7579590 | 7579591 | 7579591 | Splice_Site | C | T | p.S33_splice |
| LIHC | TCGA-UB-A7MD-01 | exon_skip_286384 | 7579312 | 7579590 | 7579591 | 7579591 | Splice_Site | C | T | . |
| READ | TCGA-AF-2693-01 | exon_skip_286384 | 7579312 | 7579590 | 7579591 | 7579591 | Splice_Site | C | T | . |
| READ | TCGA-AG-3731-01 | exon_skip_286384 | 7579312 | 7579590 | 7579591 | 7579591 | Splice_Site | C | T | . |
| READ | TCGA-DC-6157-01 | exon_skip_286384 | 7579312 | 7579590 | 7579591 | 7579591 | Splice_Site | C | G | . |
| UCS | TCGA-N9-A4Q3-01 | exon_skip_286384 | 7579312 | 7579590 | 7579591 | 7579591 | Splice_Site | C | G | . |
| LGG | TCGA-DB-A4XE-01 | exon_skip_286384 | 7579312 | 7579590 | 7579592 | 7579592 | Splice_Site | T | - | . |
| OV | TCGA-24-1562-01 | exon_skip_286384 | 7579312 | 7579590 | 7579592 | 7579592 | Splice_Site | T | A | e3-2 |
| HNSC | TCGA-CQ-5326-01 | 7579700 | 7579721 | 7579698 | 7579698 | Splice_Site | A | C | p.L32_splice | |
| HNSC | TCGA-CR-7376-01 | 7579700 | 7579721 | 7579698 | 7579699 | Splice_Site | - | CC | p.L32_splice | |
| GBM | TCGA-28-5219-01 | 7579700 | 7579721 | 7579699 | 7579699 | Splice_Site | C | T | p.L32_splice | |
| KICH | TCGA-KN-8433-01 | 7579700 | 7579721 | 7579699 | 7579699 | Splice_Site | C | A | . | |
| KICH | TCGA-KN-8433-01 | 7579700 | 7579721 | 7579699 | 7579699 | Splice_Site | C | A | p.L32_splice | |
| ACC | TCGA-OR-A5JA-01 | 7579700 | 7579721 | 7579722 | 7579722 | Splice_Site | C | A | . |
| - Depth of coverage in the three exons composing exon skipping event |
| Depth of coverage in three exons | Mutation description |
 | Sample: TCGA-KN-8433-01 |
| Cancer type: KICH | |
| ESID: | |
| Skipped exon start: 7579700 | |
| Skipped exon end: 7579721 | |
| Mutation start: 7579699 | |
| Mutation end: 7579699 | |
| Mutation type: Splice_Site | |
| Reference seq: C | |
| Mutation seq: A | |
| AAchange: . | |
| Sample: TCGA-KN-8433-01 |
| Cancer type: KICH | |
| ESID: | |
| Skipped exon start: 7579700 | |
| Skipped exon end: 7579721 | |
| Mutation start: 7579699 | |
| Mutation end: 7579699 | |
| Mutation type: Splice_Site | |
| Reference seq: C | |
| Mutation seq: A | |
| AAchange: p.L32_splice | |
exon_skip_286388_KICH_TCGA-KN-8433-01.png | |
 | Sample: TCGA-A2-A0YG-01 |
| Cancer type: BRCA | |
| ESID: exon_skip_286384 | |
| Skipped exon start: 7579312 | |
| Skipped exon end: 7579590 | |
| Mutation start: 7579311 | |
| Mutation end: 7579311 | |
| Mutation type: Splice_Site | |
| Reference seq: C | |
| Mutation seq: A | |
| AAchange: e3+1 | |
exon_skip_286384_BRCA_TCGA-A2-A0YG-01.png | |
exon_skip_436294_BRCA_TCGA-A2-A0YG-01.png | |
exon_skip_436296_BRCA_TCGA-A2-A0YG-01.png | |
 | Sample: TCGA-A8-A07O-01 |
| Cancer type: BRCA | |
| ESID: exon_skip_286384 | |
| Skipped exon start: 7579312 | |
| Skipped exon end: 7579590 | |
| Mutation start: 7579311 | |
| Mutation end: 7579311 | |
| Mutation type: Splice_Site | |
| Reference seq: C | |
| Mutation seq: T | |
| AAchange: e3+1 | |
exon_skip_286384_BRCA_TCGA-A8-A07O-01.png | |
 | Sample: TCGA-E2-A155-01 |
| Cancer type: BRCA | |
| ESID: exon_skip_286384 | |
| Skipped exon start: 7579312 | |
| Skipped exon end: 7579590 | |
| Mutation start: 7579591 | |
| Mutation end: 7579591 | |
| Mutation type: Splice_Site | |
| Reference seq: C | |
| Mutation seq: G | |
| AAchange: e3-1 | |
exon_skip_286384_BRCA_TCGA-E2-A155-01.png | |
 | Sample: TCGA-CN-4740-01 |
| Cancer type: HNSC | |
| ESID: exon_skip_286384 | |
| Skipped exon start: 7579312 | |
| Skipped exon end: 7579590 | |
| Mutation start: 7579591 | |
| Mutation end: 7579591 | |
| Mutation type: Splice_Site | |
| Reference seq: C | |
| Mutation seq: T | |
| AAchange: p.S33_splice | |
exon_skip_286384_HNSC_TCGA-CN-4740-01.png | |
exon_skip_318647_HNSC_TCGA-CN-4740-01.png | |
 | Sample: TCGA-DU-7304-01 |
| Cancer type: LGG | |
| ESID: exon_skip_286384 | |
| Skipped exon start: 7579312 | |
| Skipped exon end: 7579590 | |
| Mutation start: 7579311 | |
| Mutation end: 7579311 | |
| Mutation type: Splice_Site | |
| Reference seq: C | |
| Mutation seq: - | |
| AAchange: . | |
exon_skip_286384_LGG_TCGA-DU-7304-01.png | |
 | Sample: TCGA-DU-7007-01 |
| Cancer type: LGG | |
| ESID: exon_skip_286384 | |
| Skipped exon start: 7579312 | |
| Skipped exon end: 7579590 | |
| Mutation start: 7579311 | |
| Mutation end: 7579311 | |
| Mutation type: Splice_Site | |
| Reference seq: C | |
| Mutation seq: G | |
| AAchange: . | |
exon_skip_286384_LGG_TCGA-DU-7007-01.png | |
 | Sample: TCGA-DB-A4XE-01 |
| Cancer type: LGG | |
| ESID: exon_skip_286384 | |
| Skipped exon start: 7579312 | |
| Skipped exon end: 7579590 | |
| Mutation start: 7579592 | |
| Mutation end: 7579592 | |
| Mutation type: Splice_Site | |
| Reference seq: T | |
| Mutation seq: - | |
| AAchange: . | |
exon_skip_286384_LGG_TCGA-DB-A4XE-01.png | |
 | Sample: TCGA-UB-A7MD-01 |
| Cancer type: LIHC | |
| ESID: exon_skip_286384 | |
| Skipped exon start: 7579312 | |
| Skipped exon end: 7579590 | |
| Mutation start: 7579591 | |
| Mutation end: 7579591 | |
| Mutation type: Splice_Site | |
| Reference seq: C | |
| Mutation seq: T | |
| AAchange: . | |
exon_skip_286384_LIHC_TCGA-UB-A7MD-01.png | |
 | Sample: TCGA-97-7938-01 |
| Cancer type: LUAD | |
| ESID: exon_skip_286384 | |
| Skipped exon start: 7579312 | |
| Skipped exon end: 7579590 | |
| Mutation start: 7579310 | |
| Mutation end: 7579310 | |
| Mutation type: Splice_Site | |
| Reference seq: A | |
| Mutation seq: T | |
| AAchange: p.T125_splice | |
exon_skip_286384_LUAD_TCGA-97-7938-01.png | |
exon_skip_491453_LUAD_TCGA-97-7938-01.png | |
exon_skip_80383_LUAD_TCGA-97-7938-01.png | |
 | Sample: TCGA-34-5239-01 |
| Cancer type: LUSC | |
| ESID: exon_skip_286384 | |
| Skipped exon start: 7579312 | |
| Skipped exon end: 7579590 | |
| Mutation start: 7579311 | |
| Mutation end: 7579311 | |
| Mutation type: Splice_Site | |
| Reference seq: C | |
| Mutation seq: A | |
| AAchange: p.T125_splice | |
exon_skip_286384_LUSC_TCGA-34-5239-01.png | |
 | Sample: TCGA-66-2788-01 |
| Cancer type: LUSC | |
| ESID: exon_skip_286384 | |
| Skipped exon start: 7579312 | |
| Skipped exon end: 7579590 | |
| Mutation start: 7579311 | |
| Mutation end: 7579311 | |
| Mutation type: Splice_Site | |
| Reference seq: C | |
| Mutation seq: A | |
| AAchange: p.T125_splice | |
exon_skip_286384_LUSC_TCGA-66-2788-01.png | |
 | Sample: TCGA-13-1403-01 |
| Cancer type: OV | |
| ESID: exon_skip_286384 | |
| Skipped exon start: 7579312 | |
| Skipped exon end: 7579590 | |
| Mutation start: 7579311 | |
| Mutation end: 7579311 | |
| Mutation type: Splice_Site | |
| Reference seq: C | |
| Mutation seq: A | |
| AAchange: e3+1 | |
exon_skip_286384_OV_TCGA-13-1403-01.png | |
 | Sample: TCGA-24-1562-01 |
| Cancer type: OV | |
| ESID: exon_skip_286384 | |
| Skipped exon start: 7579312 | |
| Skipped exon end: 7579590 | |
| Mutation start: 7579592 | |
| Mutation end: 7579592 | |
| Mutation type: Splice_Site | |
| Reference seq: T | |
| Mutation seq: A | |
| AAchange: e3-2 | |
exon_skip_286384_OV_TCGA-24-1562-01.png | |
exon_skip_70828_OV_TCGA-24-1562-01.png | |
 | Sample: TCGA-IB-7649-01 |
| Cancer type: PAAD | |
| ESID: exon_skip_286384 | |
| Skipped exon start: 7579312 | |
| Skipped exon end: 7579590 | |
| Mutation start: 7579311 | |
| Mutation end: 7579311 | |
| Mutation type: Splice_Site | |
| Reference seq: C | |
| Mutation seq: T | |
| AAchange: . | |
exon_skip_286384_PAAD_TCGA-IB-7649-01.png | |
 | Sample: TCGA-DC-6157-01 |
| Cancer type: READ | |
| ESID: exon_skip_286384 | |
| Skipped exon start: 7579312 | |
| Skipped exon end: 7579590 | |
| Mutation start: 7579591 | |
| Mutation end: 7579591 | |
| Mutation type: Splice_Site | |
| Reference seq: C | |
| Mutation seq: G | |
| AAchange: . | |
exon_skip_286384_READ_TCGA-DC-6157-01.png | |
 | Sample: TCGA-AF-2693-01 |
| Cancer type: READ | |
| ESID: exon_skip_286384 | |
| Skipped exon start: 7579312 | |
| Skipped exon end: 7579590 | |
| Mutation start: 7579591 | |
| Mutation end: 7579591 | |
| Mutation type: Splice_Site | |
| Reference seq: C | |
| Mutation seq: T | |
| AAchange: . | |
exon_skip_286384_READ_TCGA-AF-2693-01.png | |
 | Sample: TCGA-AG-3731-01 |
| Cancer type: READ | |
| ESID: exon_skip_286384 | |
| Skipped exon start: 7579312 | |
| Skipped exon end: 7579590 | |
| Mutation start: 7579591 | |
| Mutation end: 7579591 | |
| Mutation type: Splice_Site | |
| Reference seq: C | |
| Mutation seq: T | |
| AAchange: . | |
exon_skip_286384_READ_TCGA-AG-3731-01.png | |
 | Sample: TCGA-EE-A2MQ-06 |
| Cancer type: SKCM | |
| ESID: exon_skip_286384 | |
| Skipped exon start: 7579312 | |
| Skipped exon end: 7579590 | |
| Mutation start: 7579310 | |
| Mutation end: 7579310 | |
| Mutation type: Splice_Site | |
| Reference seq: A | |
| Mutation seq: G | |
| AAchange: . | |
exon_skip_286384_SKCM_TCGA-EE-A2MQ-06.png | |
 | Sample: TCGA-BR-8369-01 |
| Cancer type: STAD | |
| ESID: exon_skip_286384 | |
| Skipped exon start: 7579312 | |
| Skipped exon end: 7579590 | |
| Mutation start: 7579311 | |
| Mutation end: 7579311 | |
| Mutation type: Splice_Site | |
| Reference seq: C | |
| Mutation seq: T | |
| AAchange: . | |
| Sample: TCGA-BR-8369-01 |
| Cancer type: STAD | |
| ESID: exon_skip_286384 | |
| Skipped exon start: 7579312 | |
| Skipped exon end: 7579590 | |
| Mutation start: 7579311 | |
| Mutation end: 7579311 | |
| Mutation type: Splice_Site | |
| Reference seq: C | |
| Mutation seq: T | |
| AAchange: p.T125_splice | |
exon_skip_286384_STAD_TCGA-BR-8369-01.png | |
 | Sample: TCGA-BR-8483-01 |
| Cancer type: STAD | |
| ESID: exon_skip_286384 | |
| Skipped exon start: 7579312 | |
| Skipped exon end: 7579590 | |
| Mutation start: 7579311 | |
| Mutation end: 7579311 | |
| Mutation type: Splice_Site | |
| Reference seq: C | |
| Mutation seq: T | |
| AAchange: . | |
| Sample: TCGA-BR-8483-01 |
| Cancer type: STAD | |
| ESID: exon_skip_286384 | |
| Skipped exon start: 7579312 | |
| Skipped exon end: 7579590 | |
| Mutation start: 7579311 | |
| Mutation end: 7579311 | |
| Mutation type: Splice_Site | |
| Reference seq: C | |
| Mutation seq: T | |
| AAchange: p.T125_splice | |
exon_skip_286384_STAD_TCGA-BR-8483-01.png | |
 | Sample: TCGA-N9-A4Q3-01 |
| Cancer type: UCS | |
| ESID: exon_skip_286384 | |
| Skipped exon start: 7579312 | |
| Skipped exon end: 7579590 | |
| Mutation start: 7579591 | |
| Mutation end: 7579591 | |
| Mutation type: Splice_Site | |
| Reference seq: C | |
| Mutation seq: G | |
| AAchange: . | |
exon_skip_286384_UCS_TCGA-N9-A4Q3-01.png | |
 | Sample: TCGA-AR-A254-01 |
| Cancer type: BRCA | |
| ESID: exon_skip_286384 | |
| Skipped exon start: 7579312 | |
| Skipped exon end: 7579590 | |
| Mutation start: 7579315 | |
| Mutation end: 7579315 | |
| Mutation type: Nonsense_Mutation | |
| Reference seq: G | |
| Mutation seq: T | |
| AAchange: p.C124* | |
exon_skip_286384_BRCA_TCGA-AR-A254-01.png | |
 | Sample: TCGA-E9-A243-01 |
| Cancer type: BRCA | |
| ESID: exon_skip_286384 | |
| Skipped exon start: 7579312 | |
| Skipped exon end: 7579590 | |
| Mutation start: 7579414 | |
| Mutation end: 7579414 | |
| Mutation type: Nonsense_Mutation | |
| Reference seq: C | |
| Mutation seq: T | |
| AAchange: p.W91* | |
exon_skip_286384_BRCA_TCGA-E9-A243-01.png | |
 | Sample: TCGA-B6-A0WX-01 |
| Cancer type: BRCA | |
| ESID: exon_skip_286384 | |
| Skipped exon start: 7579312 | |
| Skipped exon end: 7579590 | |
| Mutation start: 7579346 | |
| Mutation end: 7579346 | |
| Mutation type: Nonsense_Mutation | |
| Reference seq: A | |
| Mutation seq: T | |
| AAchange: p.L114* | |
exon_skip_286384_BRCA_TCGA-B6-A0WX-01.png | |
 | Sample: TCGA-BH-A18V-01 |
| Cancer type: BRCA | |
| ESID: exon_skip_286384 | |
| Skipped exon start: 7579312 | |
| Skipped exon end: 7579590 | |
| Mutation start: 7579521 | |
| Mutation end: 7579521 | |
| Mutation type: Nonsense_Mutation | |
| Reference seq: C | |
| Mutation seq: A | |
| AAchange: p.E56* | |
exon_skip_286384_BRCA_TCGA-BH-A18V-01.png | |
 | Sample: TCGA-CM-6172-01 |
| Cancer type: COAD | |
| ESID: exon_skip_286384 | |
| Skipped exon start: 7579312 | |
| Skipped exon end: 7579590 | |
| Mutation start: 7579389 | |
| Mutation end: 7579389 | |
| Mutation type: Nonsense_Mutation | |
| Reference seq: G | |
| Mutation seq: A | |
| AAchange: p.Q100X | |
exon_skip_286384_COAD_TCGA-CM-6172-01.png | |
 | Sample: TCGA-CA-6718-01 |
| Cancer type: COAD | |
| ESID: exon_skip_286384 | |
| Skipped exon start: 7579312 | |
| Skipped exon end: 7579590 | |
| Mutation start: 7579406 | |
| Mutation end: 7579406 | |
| Mutation type: Nonsense_Mutation | |
| Reference seq: G | |
| Mutation seq: T | |
| AAchange: p.S94X | |
exon_skip_141986_COAD_TCGA-CA-6718-01.png | |
exon_skip_149207_COAD_TCGA-CA-6718-01.png | |
exon_skip_286384_COAD_TCGA-CA-6718-01.png | |
exon_skip_30232_COAD_TCGA-CA-6718-01.png | |
exon_skip_30235_COAD_TCGA-CA-6718-01.png | |
exon_skip_317435_COAD_TCGA-CA-6718-01.png | |
exon_skip_317461_COAD_TCGA-CA-6718-01.png | |
exon_skip_387073_COAD_TCGA-CA-6718-01.png | |
exon_skip_44936_COAD_TCGA-CA-6718-01.png | |
exon_skip_501551_COAD_TCGA-CA-6718-01.png | |
exon_skip_86037_COAD_TCGA-CA-6718-01.png | |
 | Sample: TCGA-CM-5860-01 |
| Cancer type: COAD | |
| ESID: exon_skip_286384 | |
| Skipped exon start: 7579312 | |
| Skipped exon end: 7579590 | |
| Mutation start: 7579415 | |
| Mutation end: 7579415 | |
| Mutation type: Nonsense_Mutation | |
| Reference seq: C | |
| Mutation seq: T | |
| AAchange: p.W91X | |
exon_skip_286384_COAD_TCGA-CM-5860-01.png | |
 | Sample: TCGA-R6-A8W8-01 |
| Cancer type: ESCA | |
| ESID: exon_skip_286384 | |
| Skipped exon start: 7579312 | |
| Skipped exon end: 7579590 | |
| Mutation start: 7579536 | |
| Mutation end: 7579536 | |
| Mutation type: Nonsense_Mutation | |
| Reference seq: C | |
| Mutation seq: A | |
| AAchange: p.E51X | |
| Sample: TCGA-R6-A8W8-01 |
| Cancer type: ESCA | |
| ESID: exon_skip_286384 | |
| Skipped exon start: 7579312 | |
| Skipped exon end: 7579590 | |
| Mutation start: 7579536 | |
| Mutation end: 7579536 | |
| Mutation type: Nonsense_Mutation | |
| Reference seq: C | |
| Mutation seq: A | |
| AAchange: p.E51* | |
exon_skip_107170_ESCA_TCGA-R6-A8W8-01.png | |
exon_skip_107867_ESCA_TCGA-R6-A8W8-01.png | |
exon_skip_286384_ESCA_TCGA-R6-A8W8-01.png | |
exon_skip_70600_ESCA_TCGA-R6-A8W8-01.png | |
 | Sample: TCGA-R6-A8WC-01 |
| Cancer type: ESCA | |
| ESID: exon_skip_286384 | |
| Skipped exon start: 7579312 | |
| Skipped exon end: 7579590 | |
| Mutation start: 7579414 | |
| Mutation end: 7579414 | |
| Mutation type: Nonsense_Mutation | |
| Reference seq: C | |
| Mutation seq: T | |
| AAchange: p.W91X | |
| Sample: TCGA-R6-A8WC-01 |
| Cancer type: ESCA | |
| ESID: exon_skip_286384 | |
| Skipped exon start: 7579312 | |
| Skipped exon end: 7579590 | |
| Mutation start: 7579414 | |
| Mutation end: 7579414 | |
| Mutation type: Nonsense_Mutation | |
| Reference seq: C | |
| Mutation seq: T | |
| AAchange: p.W91* | |
exon_skip_286384_ESCA_TCGA-R6-A8WC-01.png | |
exon_skip_288276_ESCA_TCGA-R6-A8WC-01.png | |
exon_skip_367235_ESCA_TCGA-R6-A8WC-01.png | |
 | Sample: TCGA-VR-AA4G-01 |
| Cancer type: ESCA | |
| ESID: exon_skip_286384 | |
| Skipped exon start: 7579312 | |
| Skipped exon end: 7579590 | |
| Mutation start: 7579406 | |
| Mutation end: 7579406 | |
| Mutation type: Nonsense_Mutation | |
| Reference seq: G | |
| Mutation seq: T | |
| AAchange: p.S94X | |
| Sample: TCGA-VR-AA4G-01 |
| Cancer type: ESCA | |
| ESID: exon_skip_286384 | |
| Skipped exon start: 7579312 | |
| Skipped exon end: 7579590 | |
| Mutation start: 7579406 | |
| Mutation end: 7579406 | |
| Mutation type: Nonsense_Mutation | |
| Reference seq: G | |
| Mutation seq: T | |
| AAchange: p.S94* | |
exon_skip_286384_ESCA_TCGA-VR-AA4G-01.png | |
 | Sample: TCGA-CV-7252-01 |
| Cancer type: HNSC | |
| ESID: exon_skip_286379 | |
| Skipped exon start: 7578177 | |
| Skipped exon end: 7578289 | |
| Mutation start: 7578267 | |
| Mutation end: 7578268 | |
| Mutation type: Frame_Shift_Ins | |
| Reference seq: - | |
| Mutation seq: AG | |
| AAchange: p.H194fs | |
| Sample: TCGA-CV-7252-01 |
| Cancer type: HNSC | |
| ESID: exon_skip_286379 | |
| Skipped exon start: 7578177 | |
| Skipped exon end: 7578289 | |
| Mutation start: 7578267 | |
| Mutation end: 7578268 | |
| Mutation type: Frame_Shift_Ins | |
| Reference seq: - | |
| Mutation seq: AG | |
| AAchange: p.L194fs | |
| Sample: TCGA-CV-7252-01 |
| Cancer type: HNSC | |
| ESID: exon_skip_286384 | |
| Skipped exon start: 7579312 | |
| Skipped exon end: 7579590 | |
| Mutation start: 7579533 | |
| Mutation end: 7579533 | |
| Mutation type: Nonsense_Mutation | |
| Reference seq: G | |
| Mutation seq: A | |
| AAchange: p.Q52* | |
exon_skip_286384_HNSC_TCGA-CV-7252-01.png | |
 | Sample: TCGA-CV-7422-01 |
| Cancer type: HNSC | |
| ESID: exon_skip_286384 | |
| Skipped exon start: 7579312 | |
| Skipped exon end: 7579590 | |
| Mutation start: 7579377 | |
| Mutation end: 7579377 | |
| Mutation type: Nonsense_Mutation | |
| Reference seq: G | |
| Mutation seq: A | |
| AAchange: p.Q104* | |
exon_skip_286384_HNSC_TCGA-CV-7422-01.png | |
 | Sample: TCGA-CV-7263-01 |
| Cancer type: HNSC | |
| ESID: exon_skip_286384 | |
| Skipped exon start: 7579312 | |
| Skipped exon end: 7579590 | |
| Mutation start: 7579378 | |
| Mutation end: 7579378 | |
| Mutation type: Nonsense_Mutation | |
| Reference seq: G | |
| Mutation seq: C | |
| AAchange: p.Y103* | |
exon_skip_15182_HNSC_TCGA-CV-7263-01.png | |
exon_skip_286384_HNSC_TCGA-CV-7263-01.png | |
 | Sample: TCGA-CV-5436-01 |
| Cancer type: HNSC | |
| ESID: exon_skip_286384 | |
| Skipped exon start: 7579312 | |
| Skipped exon end: 7579590 | |
| Mutation start: 7579521 | |
| Mutation end: 7579521 | |
| Mutation type: Nonsense_Mutation | |
| Reference seq: C | |
| Mutation seq: A | |
| AAchange: p.E56* | |
exon_skip_286384_HNSC_TCGA-CV-5436-01.png | |
 | Sample: TCGA-UF-A7JA-01 |
| Cancer type: HNSC | |
| ESID: exon_skip_286384 | |
| Skipped exon start: 7579312 | |
| Skipped exon end: 7579590 | |
| Mutation start: 7579485 | |
| Mutation end: 7579485 | |
| Mutation type: Nonsense_Mutation | |
| Reference seq: C | |
| Mutation seq: A | |
| AAchange: p.E68* | |
exon_skip_286384_HNSC_TCGA-UF-A7JA-01.png | |
 | Sample: TCGA-CV-7104-01 |
| Cancer type: HNSC | |
| ESID: exon_skip_286384 | |
| Skipped exon start: 7579312 | |
| Skipped exon end: 7579590 | |
| Mutation start: 7579575 | |
| Mutation end: 7579575 | |
| Mutation type: Nonsense_Mutation | |
| Reference seq: G | |
| Mutation seq: A | |
| AAchange: p.Q38* | |
exon_skip_286384_HNSC_TCGA-CV-7104-01.png | |
exon_skip_4028_HNSC_TCGA-CV-7104-01.png | |
 | Sample: TCGA-D6-A74Q-01 |
| Cancer type: HNSC | |
| ESID: exon_skip_286384 | |
| Skipped exon start: 7579312 | |
| Skipped exon end: 7579590 | |
| Mutation start: 7579485 | |
| Mutation end: 7579485 | |
| Mutation type: Nonsense_Mutation | |
| Reference seq: C | |
| Mutation seq: A | |
| AAchange: p.E68* | |
exon_skip_286384_HNSC_TCGA-D6-A74Q-01.png | |
 | Sample: TCGA-H7-8501-01 |
| Cancer type: HNSC | |
| ESID: exon_skip_286384 | |
| Skipped exon start: 7579312 | |
| Skipped exon end: 7579590 | |
| Mutation start: 7579521 | |
| Mutation end: 7579521 | |
| Mutation type: Nonsense_Mutation | |
| Reference seq: C | |
| Mutation seq: A | |
| AAchange: p.E56* | |
exon_skip_286384_HNSC_TCGA-H7-8501-01.png | |
 | Sample: TCGA-B3-4104-01 |
| Cancer type: KIRP | |
| ESID: exon_skip_286384 | |
| Skipped exon start: 7579312 | |
| Skipped exon end: 7579590 | |
| Mutation start: 7579415 | |
| Mutation end: 7579415 | |
| Mutation type: Nonsense_Mutation | |
| Reference seq: C | |
| Mutation seq: T | |
| AAchange: p.W91X | |
| Sample: TCGA-B3-4104-01 |
| Cancer type: KIRP | |
| ESID: exon_skip_286384 | |
| Skipped exon start: 7579312 | |
| Skipped exon end: 7579590 | |
| Mutation start: 7579415 | |
| Mutation end: 7579415 | |
| Mutation type: Nonsense_Mutation | |
| Reference seq: C | |
| Mutation seq: T | |
| AAchange: p.W91* | |
exon_skip_127618_KIRP_TCGA-B3-4104-01.png | |
exon_skip_286384_KIRP_TCGA-B3-4104-01.png | |
 | Sample: TCGA-44-7662-01 |
| Cancer type: LUAD | |
| ESID: exon_skip_286384 | |
| Skipped exon start: 7579312 | |
| Skipped exon end: 7579590 | |
| Mutation start: 7579485 | |
| Mutation end: 7579485 | |
| Mutation type: Nonsense_Mutation | |
| Reference seq: C | |
| Mutation seq: A | |
| AAchange: p.E68* | |
exon_skip_286384_LUAD_TCGA-44-7662-01.png | |
 | Sample: TCGA-44-A4SU-01 |
| Cancer type: LUAD | |
| ESID: exon_skip_286384 | |
| Skipped exon start: 7579312 | |
| Skipped exon end: 7579590 | |
| Mutation start: 7579528 | |
| Mutation end: 7579528 | |
| Mutation type: Nonsense_Mutation | |
| Reference seq: C | |
| Mutation seq: T | |
| AAchange: p.W53* | |
exon_skip_286384_LUAD_TCGA-44-A4SU-01.png | |
 | Sample: TCGA-50-5931-01 |
| Cancer type: LUAD | |
| ESID: exon_skip_286384 | |
| Skipped exon start: 7579312 | |
| Skipped exon end: 7579590 | |
| Mutation start: 7579414 | |
| Mutation end: 7579414 | |
| Mutation type: Nonsense_Mutation | |
| Reference seq: C | |
| Mutation seq: T | |
| AAchange: p.W91* | |
exon_skip_286384_LUAD_TCGA-50-5931-01.png | |
 | Sample: TCGA-21-5784-01 |
| Cancer type: LUSC | |
| ESID: exon_skip_286384 | |
| Skipped exon start: 7579312 | |
| Skipped exon end: 7579590 | |
| Mutation start: 7579414 | |
| Mutation end: 7579414 | |
| Mutation type: Nonsense_Mutation | |
| Reference seq: C | |
| Mutation seq: T | |
| AAchange: p.W91* | |
exon_skip_286384_LUSC_TCGA-21-5784-01.png | |
exon_skip_478451_LUSC_TCGA-21-5784-01.png | |
 | Sample: TCGA-39-5031-01 |
| Cancer type: LUSC | |
| ESID: exon_skip_286384 | |
| Skipped exon start: 7579312 | |
| Skipped exon end: 7579590 | |
| Mutation start: 7579378 | |
| Mutation end: 7579378 | |
| Mutation type: Nonsense_Mutation | |
| Reference seq: G | |
| Mutation seq: T | |
| AAchange: p.Y103* | |
exon_skip_106744_LUSC_TCGA-39-5031-01.png | |
exon_skip_286384_LUSC_TCGA-39-5031-01.png | |
exon_skip_390779_LUSC_TCGA-39-5031-01.png | |
 | Sample: TCGA-2L-AAQE-01 |
| Cancer type: PAAD | |
| ESID: exon_skip_286384 | |
| Skipped exon start: 7579312 | |
| Skipped exon end: 7579590 | |
| Mutation start: 7579575 | |
| Mutation end: 7579575 | |
| Mutation type: Nonsense_Mutation | |
| Reference seq: G | |
| Mutation seq: A | |
| AAchange: p.Q38X | |
| Sample: TCGA-2L-AAQE-01 |
| Cancer type: PAAD | |
| ESID: exon_skip_286384 | |
| Skipped exon start: 7579312 | |
| Skipped exon end: 7579590 | |
| Mutation start: 7579575 | |
| Mutation end: 7579575 | |
| Mutation type: Nonsense_Mutation | |
| Reference seq: G | |
| Mutation seq: A | |
| AAchange: p.Q38* | |
exon_skip_286384_PAAD_TCGA-2L-AAQE-01.png | |
 | Sample: TCGA-G5-6235-01 |
| Cancer type: READ | |
| ESID: exon_skip_286384 | |
| Skipped exon start: 7579312 | |
| Skipped exon end: 7579590 | |
| Mutation start: 7579536 | |
| Mutation end: 7579536 | |
| Mutation type: Nonsense_Mutation | |
| Reference seq: C | |
| Mutation seq: A | |
| AAchange: p.E51X | |
exon_skip_286384_READ_TCGA-G5-6235-01.png | |
 | Sample: TCGA-HS-A5N9-01 |
| Cancer type: SARC | |
| ESID: exon_skip_286384 | |
| Skipped exon start: 7579312 | |
| Skipped exon end: 7579590 | |
| Mutation start: 7579521 | |
| Mutation end: 7579521 | |
| Mutation type: Nonsense_Mutation | |
| Reference seq: C | |
| Mutation seq: A | |
| AAchange: p.E56* | |
exon_skip_286384_SARC_TCGA-HS-A5N9-01.png | |
 | Sample: TCGA-3B-A9HT-01 |
| Cancer type: SARC | |
| ESID: exon_skip_286384 | |
| Skipped exon start: 7579312 | |
| Skipped exon end: 7579590 | |
| Mutation start: 7579414 | |
| Mutation end: 7579414 | |
| Mutation type: Nonsense_Mutation | |
| Reference seq: C | |
| Mutation seq: T | |
| AAchange: p.W91* | |
exon_skip_141552_SARC_TCGA-3B-A9HT-01.png | |
exon_skip_286384_SARC_TCGA-3B-A9HT-01.png | |
exon_skip_377825_SARC_TCGA-3B-A9HT-01.png | |
exon_skip_51238_SARC_TCGA-3B-A9HT-01.png | |
 | Sample: TCGA-BR-8678-01 |
| Cancer type: STAD | |
| ESID: exon_skip_286384 | |
| Skipped exon start: 7579312 | |
| Skipped exon end: 7579590 | |
| Mutation start: 7579406 | |
| Mutation end: 7579406 | |
| Mutation type: Nonsense_Mutation | |
| Reference seq: G | |
| Mutation seq: C | |
| AAchange: p.S94X | |
| Sample: TCGA-BR-8678-01 |
| Cancer type: STAD | |
| ESID: exon_skip_286384 | |
| Skipped exon start: 7579312 | |
| Skipped exon end: 7579590 | |
| Mutation start: 7579406 | |
| Mutation end: 7579406 | |
| Mutation type: Nonsense_Mutation | |
| Reference seq: G | |
| Mutation seq: C | |
| AAchange: p.S94* | |
exon_skip_286384_STAD_TCGA-BR-8678-01.png | |
 | Sample: TCGA-N8-A56S-01 |
| Cancer type: UCS | |
| ESID: exon_skip_286384 | |
| Skipped exon start: 7579312 | |
| Skipped exon end: 7579590 | |
| Mutation start: 7579389 | |
| Mutation end: 7579389 | |
| Mutation type: Nonsense_Mutation | |
| Reference seq: G | |
| Mutation seq: A | |
| AAchange: p.Q100X | |
| Sample: TCGA-N8-A56S-01 |
| Cancer type: UCS | |
| ESID: exon_skip_286384 | |
| Skipped exon start: 7579312 | |
| Skipped exon end: 7579590 | |
| Mutation start: 7579389 | |
| Mutation end: 7579389 | |
| Mutation type: Nonsense_Mutation | |
| Reference seq: G | |
| Mutation seq: A | |
| AAchange: p.Q100* | |
exon_skip_286384_UCS_TCGA-N8-A56S-01.png | |
 | Sample: TCGA-AR-A256-01 |
| Cancer type: BRCA | |
| ESID: exon_skip_286384 | |
| Skipped exon start: 7579312 | |
| Skipped exon end: 7579590 | |
| Mutation start: 7579359 | |
| Mutation end: 7579360 | |
| Mutation type: Frame_Shift_Ins | |
| Reference seq: - | |
| Mutation seq: GA | |
| AAchange: p.R109fs | |
exon_skip_286384_BRCA_TCGA-AR-A256-01.png | |
exon_skip_80665_BRCA_TCGA-AR-A256-01.png | |
 | Sample: TCGA-AR-A24K-01 |
| Cancer type: BRCA | |
| ESID: exon_skip_286384 | |
| Skipped exon start: 7579312 | |
| Skipped exon end: 7579590 | |
| Mutation start: 7579360 | |
| Mutation end: 7579361 | |
| Mutation type: Frame_Shift_Ins | |
| Reference seq: - | |
| Mutation seq: AA | |
| AAchange: p.R110fs | |
exon_skip_286384_BRCA_TCGA-AR-A24K-01.png | |
 | Sample: TCGA-D8-A27H-01 |
| Cancer type: BRCA | |
| ESID: exon_skip_286384 | |
| Skipped exon start: 7579312 | |
| Skipped exon end: 7579590 | |
| Mutation start: 7579360 | |
| Mutation end: 7579364 | |
| Mutation type: Frame_Shift_Del | |
| Reference seq: GAAAC | |
| Mutation seq: - | |
| AAchange: p.G108fs | |
exon_skip_286384_BRCA_TCGA-D8-A27H-01.png | |
exon_skip_433327_BRCA_TCGA-D8-A27H-01.png | |
 | Sample: TCGA-AR-A1AY-01 |
| Cancer type: BRCA | |
| ESID: exon_skip_286384 | |
| Skipped exon start: 7579312 | |
| Skipped exon end: 7579590 | |
| Mutation start: 7579321 | |
| Mutation end: 7579322 | |
| Mutation type: Frame_Shift_Del | |
| Reference seq: CA | |
| Mutation seq: - | |
| AAchange: p.V122fs | |
exon_skip_286384_BRCA_TCGA-AR-A1AY-01.png | |
 | Sample: TCGA-AR-A1AN-01 |
| Cancer type: BRCA | |
| ESID: exon_skip_286384 | |
| Skipped exon start: 7579312 | |
| Skipped exon end: 7579590 | |
| Mutation start: 7579359 | |
| Mutation end: 7579359 | |
| Mutation type: Frame_Shift_Del | |
| Reference seq: G | |
| Mutation seq: - | |
| AAchange: p.R110fs | |
exon_skip_286384_BRCA_TCGA-AR-A1AN-01.png | |
 | Sample: TCGA-BH-A0C0-01 |
| Cancer type: BRCA | |
| ESID: exon_skip_286384 | |
| Skipped exon start: 7579312 | |
| Skipped exon end: 7579590 | |
| Mutation start: 7579359 | |
| Mutation end: 7579359 | |
| Mutation type: Frame_Shift_Del | |
| Reference seq: G | |
| Mutation seq: - | |
| AAchange: p.R110fs | |
exon_skip_138095_BRCA_TCGA-BH-A0C0-01.png | |
exon_skip_286384_BRCA_TCGA-BH-A0C0-01.png | |
 | Sample: TCGA-AN-A0AJ-01 |
| Cancer type: BRCA | |
| ESID: exon_skip_286384 | |
| Skipped exon start: 7579312 | |
| Skipped exon end: 7579590 | |
| Mutation start: 7579364 | |
| Mutation end: 7579364 | |
| Mutation type: Frame_Shift_Del | |
| Reference seq: C | |
| Mutation seq: - | |
| AAchange: p.G108fs | |
exon_skip_286384_BRCA_TCGA-AN-A0AJ-01.png | |
 | Sample: TCGA-BH-A18Q-01 |
| Cancer type: BRCA | |
| ESID: exon_skip_286384 | |
| Skipped exon start: 7579312 | |
| Skipped exon end: 7579590 | |
| Mutation start: 7579458 | |
| Mutation end: 7579459 | |
| Mutation type: Frame_Shift_Ins | |
| Reference seq: - | |
| Mutation seq: TGCA | |
| AAchange: p.P76fs | |
exon_skip_286384_BRCA_TCGA-BH-A18Q-01.png | |
exon_skip_455061_BRCA_TCGA-BH-A18Q-01.png | |
exon_skip_479254_BRCA_TCGA-BH-A18Q-01.png | |
 | Sample: TCGA-VR-A8EY-01 |
| Cancer type: ESCA | |
| ESID: exon_skip_286384 | |
| Skipped exon start: 7579312 | |
| Skipped exon end: 7579590 | |
| Mutation start: 7579563 | |
| Mutation end: 7579563 | |
| Mutation type: Frame_Shift_Del | |
| Reference seq: C | |
| Mutation seq: - | |
| AAchange: p.D42fs | |
exon_skip_124728_ESCA_TCGA-VR-A8EY-01.png | |
exon_skip_126584_ESCA_TCGA-VR-A8EY-01.png | |
exon_skip_286384_ESCA_TCGA-VR-A8EY-01.png | |
exon_skip_323786_ESCA_TCGA-VR-A8EY-01.png | |
exon_skip_323787_ESCA_TCGA-VR-A8EY-01.png | |
exon_skip_423700_ESCA_TCGA-VR-A8EY-01.png | |
exon_skip_423701_ESCA_TCGA-VR-A8EY-01.png | |
 | Sample: TCGA-LN-A5U6-01 |
| Cancer type: ESCA | |
| ESID: exon_skip_286384 | |
| Skipped exon start: 7579312 | |
| Skipped exon end: 7579590 | |
| Mutation start: 7579497 | |
| Mutation end: 7579498 | |
| Mutation type: Frame_Shift_Del | |
| Reference seq: GA | |
| Mutation seq: - | |
| AAchange: p.64_64del | |
| Sample: TCGA-LN-A5U6-01 |
| Cancer type: ESCA | |
| ESID: exon_skip_286384 | |
| Skipped exon start: 7579312 | |
| Skipped exon end: 7579590 | |
| Mutation start: 7579497 | |
| Mutation end: 7579498 | |
| Mutation type: Frame_Shift_Del | |
| Reference seq: GA | |
| Mutation seq: - | |
| AAchange: p.AP63fs | |
| Sample: TCGA-LN-A5U6-01 |
| Cancer type: ESCA | |
| ESID: exon_skip_286384 | |
| Skipped exon start: 7579312 | |
| Skipped exon end: 7579590 | |
| Mutation start: 7579497 | |
| Mutation end: 7579498 | |
| Mutation type: Frame_Shift_Del | |
| Reference seq: GA | |
| Mutation seq: - | |
| AAchange: p.P64fs | |
exon_skip_286384_ESCA_TCGA-LN-A5U6-01.png | |
 | Sample: TCGA-2H-A9GI-01 |
| Cancer type: ESCA | |
| ESID: exon_skip_286384 | |
| Skipped exon start: 7579312 | |
| Skipped exon end: 7579590 | |
| Mutation start: 7579579 | |
| Mutation end: 7579580 | |
| Mutation type: Frame_Shift_Ins | |
| Reference seq: - | |
| Mutation seq: GGCAAGGG | |
| AAchange: p.P36fs | |
| Sample: TCGA-2H-A9GI-01 |
| Cancer type: ESCA | |
| ESID: exon_skip_286384 | |
| Skipped exon start: 7579312 | |
| Skipped exon end: 7579590 | |
| Mutation start: 7579579 | |
| Mutation end: 7579580 | |
| Mutation type: Frame_Shift_Ins | |
| Reference seq: - | |
| Mutation seq: GGCAAGGG | |
| AAchange: p.L36fs | |
exon_skip_286384_ESCA_TCGA-2H-A9GI-01.png | |
exon_skip_467473_ESCA_TCGA-2H-A9GI-01.png | |
exon_skip_467474_ESCA_TCGA-2H-A9GI-01.png | |
 | Sample: TCGA-CR-7393-01 |
| Cancer type: HNSC | |
| ESID: exon_skip_286384 | |
| Skipped exon start: 7579312 | |
| Skipped exon end: 7579590 | |
| Mutation start: 7579566 | |
| Mutation end: 7579566 | |
| Mutation type: Frame_Shift_Del | |
| Reference seq: C | |
| Mutation seq: - | |
| AAchange: p.D42fs | |
| Sample: TCGA-CR-7393-01 |
| Cancer type: HNSC | |
| ESID: exon_skip_286384 | |
| Skipped exon start: 7579312 | |
| Skipped exon end: 7579590 | |
| Mutation start: 7579566 | |
| Mutation end: 7579566 | |
| Mutation type: Frame_Shift_Del | |
| Reference seq: C | |
| Mutation seq: - | |
| AAchange: p.D41fs | |
exon_skip_286384_HNSC_TCGA-CR-7393-01.png | |
 | Sample: TCGA-CN-6017-01 |
| Cancer type: HNSC | |
| ESID: exon_skip_286384 | |
| Skipped exon start: 7579312 | |
| Skipped exon end: 7579590 | |
| Mutation start: 7579441 | |
| Mutation end: 7579453 | |
| Mutation type: Frame_Shift_Del | |
| Reference seq: CGGTGTAGGAGCT | |
| Mutation seq: - | |
| AAchange: p.AAPTP78fs | |
| Sample: TCGA-CN-6017-01 |
| Cancer type: HNSC | |
| ESID: exon_skip_286384 | |
| Skipped exon start: 7579312 | |
| Skipped exon end: 7579590 | |
| Mutation start: 7579441 | |
| Mutation end: 7579453 | |
| Mutation type: Frame_Shift_Del | |
| Reference seq: CGGTGTAGGAGCT | |
| Mutation seq: - | |
| AAchange: p.A78fs | |
exon_skip_286384_HNSC_TCGA-CN-6017-01.png | |
 | Sample: TCGA-CR-7372-01 |
| Cancer type: HNSC | |
| ESID: exon_skip_286384 | |
| Skipped exon start: 7579312 | |
| Skipped exon end: 7579590 | |
| Mutation start: 7579450 | |
| Mutation end: 7579451 | |
| Mutation type: Frame_Shift_Ins | |
| Reference seq: - | |
| Mutation seq: G | |
| AAchange: p.A79fs | |
exon_skip_286384_HNSC_TCGA-CR-7372-01.png | |
 | Sample: TCGA-CR-7389-01 |
| Cancer type: HNSC | |
| ESID: exon_skip_286384 | |
| Skipped exon start: 7579312 | |
| Skipped exon end: 7579590 | |
| Mutation start: 7579579 | |
| Mutation end: 7579579 | |
| Mutation type: Frame_Shift_Del | |
| Reference seq: C | |
| Mutation seq: - | |
| AAchange: p.P36fs | |
exon_skip_286384_HNSC_TCGA-CR-7389-01.png | |
 | Sample: TCGA-CR-7364-01 |
| Cancer type: HNSC | |
| ESID: exon_skip_286384 | |
| Skipped exon start: 7579312 | |
| Skipped exon end: 7579590 | |
| Mutation start: 7579433 | |
| Mutation end: 7579433 | |
| Mutation type: Frame_Shift_Del | |
| Reference seq: G | |
| Mutation seq: - | |
| AAchange: p.P85fs | |
exon_skip_286384_HNSC_TCGA-CR-7364-01.png | |
exon_skip_347552_HNSC_TCGA-CR-7364-01.png | |
exon_skip_347557_HNSC_TCGA-CR-7364-01.png | |
 | Sample: TCGA-C9-A47Z-01 |
| Cancer type: HNSC | |
| ESID: exon_skip_286384 | |
| Skipped exon start: 7579312 | |
| Skipped exon end: 7579590 | |
| Mutation start: 7579379 | |
| Mutation end: 7579380 | |
| Mutation type: Frame_Shift_Ins | |
| Reference seq: - | |
| Mutation seq: A | |
| AAchange: p.P103fs | |
exon_skip_286384_HNSC_TCGA-C9-A47Z-01.png | |
 | Sample: TCGA-CN-4728-01 |
| Cancer type: HNSC | |
| ESID: exon_skip_286384 | |
| Skipped exon start: 7579312 | |
| Skipped exon end: 7579590 | |
| Mutation start: 7579514 | |
| Mutation end: 7579514 | |
| Mutation type: Frame_Shift_Del | |
| Reference seq: G | |
| Mutation seq: - | |
| AAchange: p.P58fs | |
exon_skip_286384_HNSC_TCGA-CN-4728-01.png | |
 | Sample: TCGA-BA-4076-01 |
| Cancer type: HNSC | |
| ESID: exon_skip_286384 | |
| Skipped exon start: 7579312 | |
| Skipped exon end: 7579590 | |
| Mutation start: 7579470 | |
| Mutation end: 7579471 | |
| Mutation type: Frame_Shift_Ins | |
| Reference seq: - | |
| Mutation seq: G | |
| AAchange: p.G73fs | |
exon_skip_286384_HNSC_TCGA-BA-4076-01.png | |
exon_skip_379589_HNSC_TCGA-BA-4076-01.png | |
exon_skip_379590_HNSC_TCGA-BA-4076-01.png | |
exon_skip_57703_HNSC_TCGA-BA-4076-01.png | |
 | Sample: TCGA-F7-7848-01 |
| Cancer type: HNSC | |
| ESID: exon_skip_286384 | |
| Skipped exon start: 7579312 | |
| Skipped exon end: 7579590 | |
| Mutation start: 7579514 | |
| Mutation end: 7579514 | |
| Mutation type: Frame_Shift_Del | |
| Reference seq: G | |
| Mutation seq: - | |
| AAchange: p.P58fs | |
exon_skip_286384_HNSC_TCGA-F7-7848-01.png | |
exon_skip_344329_HNSC_TCGA-F7-7848-01.png | |
exon_skip_421270_HNSC_TCGA-F7-7848-01.png | |
exon_skip_456520_HNSC_TCGA-F7-7848-01.png | |
 | Sample: TCGA-CV-5430-01 |
| Cancer type: HNSC | |
| ESID: exon_skip_286384 | |
| Skipped exon start: 7579312 | |
| Skipped exon end: 7579590 | |
| Mutation start: 7579410 | |
| Mutation end: 7579420 | |
| Mutation type: Frame_Shift_Del | |
| Reference seq: GGGGCCAGGAG | |
| Mutation seq: - | |
| AAchange: p.PSWPL89fs | |
| Sample: TCGA-CV-5430-01 |
| Cancer type: HNSC | |
| ESID: exon_skip_286384 | |
| Skipped exon start: 7579312 | |
| Skipped exon end: 7579590 | |
| Mutation start: 7579410 | |
| Mutation end: 7579420 | |
| Mutation type: Frame_Shift_Del | |
| Reference seq: GGGGCCAGGAG | |
| Mutation seq: - | |
| AAchange: p.P89fs | |
exon_skip_286384_HNSC_TCGA-CV-5430-01.png | |
exon_skip_492891_HNSC_TCGA-CV-5430-01.png | |
exon_skip_78884_HNSC_TCGA-CV-5430-01.png | |
 | Sample: TCGA-BA-A6DI-01 |
| Cancer type: HNSC | |
| ESID: exon_skip_286384 | |
| Skipped exon start: 7579312 | |
| Skipped exon end: 7579590 | |
| Mutation start: 7579546 | |
| Mutation end: 7579547 | |
| Mutation type: Frame_Shift_Ins | |
| Reference seq: - | |
| Mutation seq: G | |
| AAchange: p.R47fs | |
exon_skip_286384_HNSC_TCGA-BA-A6DI-01.png | |
exon_skip_360316_HNSC_TCGA-BA-A6DI-01.png | |
 | Sample: TCGA-CV-6959-01 |
| Cancer type: HNSC | |
| ESID: exon_skip_286384 | |
| Skipped exon start: 7579312 | |
| Skipped exon end: 7579590 | |
| Mutation start: 7579390 | |
| Mutation end: 7579393 | |
| Mutation type: Frame_Shift_Del | |
| Reference seq: GGAA | |
| Mutation seq: - | |
| AAchange: p.PS98fs | |
| Sample: TCGA-CV-6959-01 |
| Cancer type: HNSC | |
| ESID: exon_skip_286384 | |
| Skipped exon start: 7579312 | |
| Skipped exon end: 7579590 | |
| Mutation start: 7579390 | |
| Mutation end: 7579393 | |
| Mutation type: Frame_Shift_Del | |
| Reference seq: GGAA | |
| Mutation seq: - | |
| AAchange: p.P98fs | |
exon_skip_286384_HNSC_TCGA-CV-6959-01.png | |
 | Sample: TCGA-FG-6689-01 |
| Cancer type: LGG | |
| ESID: exon_skip_286384 | |
| Skipped exon start: 7579312 | |
| Skipped exon end: 7579590 | |
| Mutation start: 7579589 | |
| Mutation end: 7579590 | |
| Mutation type: Frame_Shift_Ins | |
| Reference seq: - | |
| Mutation seq: A | |
| AAchange: p.S33fs | |
exon_skip_286384_LGG_TCGA-FG-6689-01.png | |
 | Sample: TCGA-TM-A7CA-01 |
| Cancer type: LGG | |
| ESID: exon_skip_286384 | |
| Skipped exon start: 7579312 | |
| Skipped exon end: 7579590 | |
| Mutation start: 7579420 | |
| Mutation end: 7579420 | |
| Mutation type: Frame_Shift_Del | |
| Reference seq: G | |
| Mutation seq: - | |
| AAchange: p.P89fs | |
| Sample: TCGA-TM-A7CA-01 |
| Cancer type: LGG | |
| ESID: exon_skip_286364 | |
| Skipped exon start: 7573927 | |
| Skipped exon end: 7574033 | |
| Mutation start: 7574003 | |
| Mutation end: 7574003 | |
| Mutation type: Nonsense_Mutation | |
| Reference seq: G | |
| Mutation seq: A | |
| AAchange: p.R342* | |
exon_skip_286384_LGG_TCGA-TM-A7CA-01.png | |
 | Sample: TCGA-QH-A6X3-01 |
| Cancer type: LGG | |
| ESID: exon_skip_286384 | |
| Skipped exon start: 7579312 | |
| Skipped exon end: 7579590 | |
| Mutation start: 7579319 | |
| Mutation end: 7579323 | |
| Mutation type: Frame_Shift_Del | |
| Reference seq: GTCAC | |
| Mutation seq: - | |
| AAchange: p.VT122fs | |
exon_skip_286384_LGG_TCGA-QH-A6X3-01.png | |
 | Sample: TCGA-TQ-A7RJ-01 |
| Cancer type: LGG | |
| ESID: exon_skip_286384 | |
| Skipped exon start: 7579312 | |
| Skipped exon end: 7579590 | |
| Mutation start: 7579328 | |
| Mutation end: 7579328 | |
| Mutation type: Frame_Shift_Del | |
| Reference seq: T | |
| Mutation seq: - | |
| AAchange: p.K120fs | |
| Sample: TCGA-TQ-A7RJ-01 |
| Cancer type: LGG | |
| ESID: exon_skip_286376 | |
| Skipped exon start: 7577019 | |
| Skipped exon end: 7577155 | |
| Mutation start: 7577022 | |
| Mutation end: 7577022 | |
| Mutation type: Nonsense_Mutation | |
| Reference seq: G | |
| Mutation seq: A | |
| AAchange: p.R306* | |
exon_skip_286384_LGG_TCGA-TQ-A7RJ-01.png | |
 | Sample: TCGA-DU-A7TA-01 |
| Cancer type: LGG | |
| ESID: exon_skip_286384 | |
| Skipped exon start: 7579312 | |
| Skipped exon end: 7579590 | |
| Mutation start: 7579323 | |
| Mutation end: 7579324 | |
| Mutation type: Frame_Shift_Ins | |
| Reference seq: - | |
| Mutation seq: A | |
| AAchange: p.D122fs | |
exon_skip_286384_LGG_TCGA-DU-A7TA-01.png | |
 | Sample: TCGA-44-5643-01 |
| Cancer type: LUAD | |
| ESID: exon_skip_286384 | |
| Skipped exon start: 7579312 | |
| Skipped exon end: 7579590 | |
| Mutation start: 7579580 | |
| Mutation end: 7579580 | |
| Mutation type: Frame_Shift_Del | |
| Reference seq: G | |
| Mutation seq: - | |
| AAchange: p.P36fs | |
exon_skip_286384_LUAD_TCGA-44-5643-01.png | |
 | Sample: TCGA-50-5941-01 |
| Cancer type: LUAD | |
| ESID: exon_skip_286384 | |
| Skipped exon start: 7579312 | |
| Skipped exon end: 7579590 | |
| Mutation start: 7579471 | |
| Mutation end: 7579471 | |
| Mutation type: Frame_Shift_Del | |
| Reference seq: G | |
| Mutation seq: - | |
| AAchange: p.P72fs | |
exon_skip_286384_LUAD_TCGA-50-5941-01.png | |
 | Sample: TCGA-55-7903-01 |
| Cancer type: LUAD | |
| ESID: exon_skip_286384 | |
| Skipped exon start: 7579312 | |
| Skipped exon end: 7579590 | |
| Mutation start: 7579583 | |
| Mutation end: 7579583 | |
| Mutation type: Frame_Shift_Del | |
| Reference seq: A | |
| Mutation seq: - | |
| AAchange: p.L35fs | |
exon_skip_286384_LUAD_TCGA-55-7903-01.png | |
exon_skip_449028_LUAD_TCGA-55-7903-01.png | |
 | Sample: TCGA-86-7953-01 |
| Cancer type: LUAD | |
| ESID: exon_skip_286384 | |
| Skipped exon start: 7579312 | |
| Skipped exon end: 7579590 | |
| Mutation start: 7579329 | |
| Mutation end: 7579345 | |
| Mutation type: Frame_Shift_Del | |
| Reference seq: TGGCTGTCCCAGAATGC | |
| Mutation seq: - | |
| AAchange: p.LHSGTAK114fs | |
exon_skip_286384_LUAD_TCGA-86-7953-01.png | |
 | Sample: TCGA-86-A4JF-01 |
| Cancer type: LUAD | |
| ESID: exon_skip_286384 | |
| Skipped exon start: 7579312 | |
| Skipped exon end: 7579590 | |
| Mutation start: 7579420 | |
| Mutation end: 7579420 | |
| Mutation type: Frame_Shift_Del | |
| Reference seq: G | |
| Mutation seq: - | |
| AAchange: p.P89fs | |
exon_skip_286384_LUAD_TCGA-86-A4JF-01.png | |
exon_skip_307494_LUAD_TCGA-86-A4JF-01.png | |
exon_skip_307495_LUAD_TCGA-86-A4JF-01.png | |
exon_skip_326432_LUAD_TCGA-86-A4JF-01.png | |
 | Sample: TCGA-91-6829-01 |
| Cancer type: LUAD | |
| ESID: exon_skip_286384 | |
| Skipped exon start: 7579312 | |
| Skipped exon end: 7579590 | |
| Mutation start: 7579471 | |
| Mutation end: 7579471 | |
| Mutation type: Frame_Shift_Del | |
| Reference seq: G | |
| Mutation seq: - | |
| AAchange: p.P72fs | |
exon_skip_286384_LUAD_TCGA-91-6829-01.png | |
exon_skip_316803_LUAD_TCGA-91-6829-01.png | |
exon_skip_388682_LUAD_TCGA-91-6829-01.png | |
exon_skip_443476_LUAD_TCGA-91-6829-01.png | |
 | Sample: TCGA-22-4593-01 |
| Cancer type: LUSC | |
| ESID: exon_skip_286384 | |
| Skipped exon start: 7579312 | |
| Skipped exon end: 7579590 | |
| Mutation start: 7579527 | |
| Mutation end: 7579542 | |
| Mutation type: Frame_Shift_Del | |
| Reference seq: ACCATTGTTCAATATC | |
| Mutation seq: - | |
| AAchange: p.D49fs | |
exon_skip_286384_LUSC_TCGA-22-4593-01.png | |
 | Sample: TCGA-51-4079-01 |
| Cancer type: LUSC | |
| ESID: exon_skip_286384 | |
| Skipped exon start: 7579312 | |
| Skipped exon end: 7579590 | |
| Mutation start: 7579545 | |
| Mutation end: 7579545 | |
| Mutation type: Frame_Shift_Del | |
| Reference seq: C | |
| Mutation seq: - | |
| AAchange: p.D48fs | |
exon_skip_286384_LUSC_TCGA-51-4079-01.png | |
 | Sample: TCGA-60-2707-01 |
| Cancer type: LUSC | |
| ESID: exon_skip_286384 | |
| Skipped exon start: 7579312 | |
| Skipped exon end: 7579590 | |
| Mutation start: 7579585 | |
| Mutation end: 7579585 | |
| Mutation type: Frame_Shift_Del | |
| Reference seq: G | |
| Mutation seq: - | |
| AAchange: p.P34fs | |
exon_skip_286384_LUSC_TCGA-60-2707-01.png | |
 | Sample: TCGA-60-2713-01 |
| Cancer type: LUSC | |
| ESID: exon_skip_286384 | |
| Skipped exon start: 7579312 | |
| Skipped exon end: 7579590 | |
| Mutation start: 7579470 | |
| Mutation end: 7579470 | |
| Mutation type: Frame_Shift_Del | |
| Reference seq: C | |
| Mutation seq: - | |
| AAchange: p.V73fs | |
exon_skip_100894_LUSC_TCGA-60-2713-01.png | |
exon_skip_286384_LUSC_TCGA-60-2713-01.png | |
exon_skip_376191_LUSC_TCGA-60-2713-01.png | |
exon_skip_388639_LUSC_TCGA-60-2713-01.png | |
 | Sample: TCGA-13-0911-01 |
| Cancer type: OV | |
| ESID: exon_skip_286384 | |
| Skipped exon start: 7579312 | |
| Skipped exon end: 7579590 | |
| Mutation start: 7579556 | |
| Mutation end: 7579560 | |
| Mutation type: Frame_Shift_Del | |
| Reference seq: ATCAA | |
| Mutation seq: - | |
| AAchange: p.L43fs | |
exon_skip_286384_OV_TCGA-13-0911-01.png | |
 | Sample: TCGA-13-1505-01 |
| Cancer type: OV | |
| ESID: exon_skip_286384 | |
| Skipped exon start: 7579312 | |
| Skipped exon end: 7579590 | |
| Mutation start: 7579462 | |
| Mutation end: 7579462 | |
| Mutation type: Frame_Shift_Del | |
| Reference seq: A | |
| Mutation seq: - | |
| AAchange: p.P75fs | |
exon_skip_286384_OV_TCGA-13-1505-01.png | |
 | Sample: TCGA-25-1320-01 |
| Cancer type: OV | |
| ESID: exon_skip_286384 | |
| Skipped exon start: 7579312 | |
| Skipped exon end: 7579590 | |
| Mutation start: 7579315 | |
| Mutation end: 7579315 | |
| Mutation type: Frame_Shift_Del | |
| Reference seq: G | |
| Mutation seq: - | |
| AAchange: p.C124fs | |
exon_skip_286384_OV_TCGA-25-1320-01.png | |
 | Sample: TCGA-25-1329-01 |
| Cancer type: OV | |
| ESID: exon_skip_286384 | |
| Skipped exon start: 7579312 | |
| Skipped exon end: 7579590 | |
| Mutation start: 7579547 | |
| Mutation end: 7579547 | |
| Mutation type: Frame_Shift_Del | |
| Reference seq: G | |
| Mutation seq: - | |
| AAchange: p.P47fs | |
exon_skip_286384_OV_TCGA-25-1329-01.png | |
 | Sample: TCGA-61-2008-01 |
| Cancer type: OV | |
| ESID: exon_skip_286384 | |
| Skipped exon start: 7579312 | |
| Skipped exon end: 7579590 | |
| Mutation start: 7579335 | |
| Mutation end: 7579336 | |
| Mutation type: Frame_Shift_Ins | |
| Reference seq: - | |
| Mutation seq: C | |
| AAchange: p.G117fs | |
exon_skip_286384_OV_TCGA-61-2008-01.png | |
 | Sample: TCGA-61-2101-01 |
| Cancer type: OV | |
| ESID: exon_skip_286384 | |
| Skipped exon start: 7579312 | |
| Skipped exon end: 7579590 | |
| Mutation start: 7579423 | |
| Mutation end: 7579432 | |
| Mutation type: Frame_Shift_Del | |
| Reference seq: GGCTGGTGCA | |
| Mutation seq: - | |
| AAchange: p.P85fs | |
exon_skip_286384_OV_TCGA-61-2101-01.png | |
 | Sample: TCGA-IB-AAUU-01 |
| Cancer type: PAAD | |
| ESID: exon_skip_286384 | |
| Skipped exon start: 7579312 | |
| Skipped exon end: 7579590 | |
| Mutation start: 7579320 | |
| Mutation end: 7579321 | |
| Mutation type: Frame_Shift_Ins | |
| Reference seq: - | |
| Mutation seq: C | |
| AAchange: p.T123fs | |
| Sample: TCGA-IB-AAUU-01 |
| Cancer type: PAAD | |
| ESID: exon_skip_286384 | |
| Skipped exon start: 7579312 | |
| Skipped exon end: 7579590 | |
| Mutation start: 7579320 | |
| Mutation end: 7579321 | |
| Mutation type: Frame_Shift_Ins | |
| Reference seq: - | |
| Mutation seq: C | |
| AAchange: p.VL122fs | |
exon_skip_148920_PAAD_TCGA-IB-AAUU-01.png | |
exon_skip_286384_PAAD_TCGA-IB-AAUU-01.png | |
 | Sample: TCGA-IB-7886-01 |
| Cancer type: PAAD | |
| ESID: exon_skip_286384 | |
| Skipped exon start: 7579312 | |
| Skipped exon end: 7579590 | |
| Mutation start: 7579518 | |
| Mutation end: 7579519 | |
| Mutation type: Frame_Shift_Ins | |
| Reference seq: - | |
| Mutation seq: TT | |
| AAchange: p.D57fs | |
| Sample: TCGA-IB-7886-01 |
| Cancer type: PAAD | |
| ESID: exon_skip_286384 | |
| Skipped exon start: 7579312 | |
| Skipped exon end: 7579590 | |
| Mutation start: 7579518 | |
| Mutation end: 7579519 | |
| Mutation type: Frame_Shift_Ins | |
| Reference seq: - | |
| Mutation seq: TT | |
| AAchange: p.P57fs | |
exon_skip_286384_PAAD_TCGA-IB-7886-01.png | |
 | Sample: TCGA-FB-AAQ1-01 |
| Cancer type: PAAD | |
| ESID: exon_skip_286384 | |
| Skipped exon start: 7579312 | |
| Skipped exon end: 7579590 | |
| Mutation start: 7579470 | |
| Mutation end: 7579471 | |
| Mutation type: Frame_Shift_Ins | |
| Reference seq: - | |
| Mutation seq: G | |
| AAchange: p.V73fs | |
| Sample: TCGA-FB-AAQ1-01 |
| Cancer type: PAAD | |
| ESID: exon_skip_286384 | |
| Skipped exon start: 7579312 | |
| Skipped exon end: 7579590 | |
| Mutation start: 7579470 | |
| Mutation end: 7579471 | |
| Mutation type: Frame_Shift_Ins | |
| Reference seq: - | |
| Mutation seq: G | |
| AAchange: p.G73fs | |
exon_skip_286384_PAAD_TCGA-FB-AAQ1-01.png | |
exon_skip_59967_PAAD_TCGA-FB-AAQ1-01.png | |
 | Sample: TCGA-3A-A9IU-01 |
| Cancer type: PAAD | |
| ESID: exon_skip_286384 | |
| Skipped exon start: 7579312 | |
| Skipped exon end: 7579590 | |
| Mutation start: 7579471 | |
| Mutation end: 7579471 | |
| Mutation type: Frame_Shift_Del | |
| Reference seq: G | |
| Mutation seq: - | |
| AAchange: p.V73fs | |
| Sample: TCGA-3A-A9IU-01 |
| Cancer type: PAAD | |
| ESID: exon_skip_286384 | |
| Skipped exon start: 7579312 | |
| Skipped exon end: 7579590 | |
| Mutation start: 7579471 | |
| Mutation end: 7579471 | |
| Mutation type: Frame_Shift_Del | |
| Reference seq: G | |
| Mutation seq: - | |
| AAchange: p.P72fs | |
exon_skip_286384_PAAD_TCGA-3A-A9IU-01.png | |
 | Sample: TCGA-2J-AABH-01 |
| Cancer type: PAAD | |
| ESID: exon_skip_286384 | |
| Skipped exon start: 7579312 | |
| Skipped exon end: 7579590 | |
| Mutation start: 7579503 | |
| Mutation end: 7579503 | |
| Mutation type: Frame_Shift_Del | |
| Reference seq: C | |
| Mutation seq: - | |
| AAchange: p.E62fs | |
exon_skip_286384_PAAD_TCGA-2J-AABH-01.png | |
 | Sample: TCGA-IB-AAUP-01 |
| Cancer type: PAAD | |
| ESID: exon_skip_286384 | |
| Skipped exon start: 7579312 | |
| Skipped exon end: 7579590 | |
| Mutation start: 7579315 | |
| Mutation end: 7579316 | |
| Mutation type: Frame_Shift_Ins | |
| Reference seq: - | |
| Mutation seq: C | |
| AAchange: p.Y124fs | |
exon_skip_286384_PAAD_TCGA-IB-AAUP-01.png | |
 | Sample: TCGA-KK-A7B4-01 |
| Cancer type: PRAD | |
| ESID: exon_skip_286384 | |
| Skipped exon start: 7579312 | |
| Skipped exon end: 7579590 | |
| Mutation start: 7579315 | |
| Mutation end: 7579316 | |
| Mutation type: Frame_Shift_Ins | |
| Reference seq: - | |
| Mutation seq: C | |
| AAchange: p.Y124fs | |
| Sample: TCGA-KK-A7B4-01 |
| Cancer type: PRAD | |
| ESID: exon_skip_286384 | |
| Skipped exon start: 7579312 | |
| Skipped exon end: 7579590 | |
| Mutation start: 7579315 | |
| Mutation end: 7579316 | |
| Mutation type: Frame_Shift_Ins | |
| Reference seq: - | |
| Mutation seq: C | |
| AAchange: p.C124fs | |
exon_skip_286384_PRAD_TCGA-KK-A7B4-01.png | |
 | Sample: TCGA-KC-A7F6-01 |
| Cancer type: PRAD | |
| ESID: exon_skip_286384 | |
| Skipped exon start: 7579312 | |
| Skipped exon end: 7579590 | |
| Mutation start: 7579402 | |
| Mutation end: 7579418 | |
| Mutation type: Frame_Shift_Del | |
| Reference seq: AGATGACAGGGGCCAGG | |
| Mutation seq: - | |
| AAchange: p.SWPLSS90fs | |
exon_skip_286384_PRAD_TCGA-KC-A7F6-01.png | |
 | Sample: TCGA-G5-6233-01 |
| Cancer type: READ | |
| ESID: exon_skip_286384 | |
| Skipped exon start: 7579312 | |
| Skipped exon end: 7579590 | |
| Mutation start: 7579316 | |
| Mutation end: 7579317 | |
| Mutation type: Frame_Shift_Ins | |
| Reference seq: - | |
| Mutation seq: AA | |
| AAchange: p.C124fs | |
exon_skip_286384_READ_TCGA-G5-6233-01.png | |
exon_skip_379758_READ_TCGA-G5-6233-01.png | |
exon_skip_462170_READ_TCGA-G5-6233-01.png | |
 | Sample: TCGA-EI-6885-01 |
| Cancer type: READ | |
| ESID: exon_skip_286384 | |
| Skipped exon start: 7579312 | |
| Skipped exon end: 7579590 | |
| Mutation start: 7579530 | |
| Mutation end: 7579531 | |
| Mutation type: Frame_Shift_Ins | |
| Reference seq: - | |
| Mutation seq: T | |
| AAchange: p.W53fs | |
exon_skip_155089_READ_TCGA-EI-6885-01.png | |
exon_skip_286384_READ_TCGA-EI-6885-01.png | |
 | Sample: TCGA-QQ-A8VF-01 |
| Cancer type: SARC | |
| ESID: exon_skip_286384 | |
| Skipped exon start: 7579312 | |
| Skipped exon end: 7579590 | |
| Mutation start: 7579321 | |
| Mutation end: 7579322 | |
| Mutation type: Frame_Shift_Del | |
| Reference seq: CA | |
| Mutation seq: - | |
| AAchange: p.V122fs | |
exon_skip_286384_SARC_TCGA-QQ-A8VF-01.png | |
exon_skip_309975_SARC_TCGA-QQ-A8VF-01.png | |
exon_skip_313776_SARC_TCGA-QQ-A8VF-01.png | |
exon_skip_358373_SARC_TCGA-QQ-A8VF-01.png | |
 | Sample: TCGA-FS-A1Z4-06 |
| Cancer type: SKCM | |
| ESID: exon_skip_286384 | |
| Skipped exon start: 7579312 | |
| Skipped exon end: 7579590 | |
| Mutation start: 7579399 | |
| Mutation end: 7579399 | |
| Mutation type: Frame_Shift_Del | |
| Reference seq: A | |
| Mutation seq: - | |
| AAchange: p.S96fs | |
exon_skip_286384_SKCM_TCGA-FS-A1Z4-06.png | |
exon_skip_385315_SKCM_TCGA-FS-A1Z4-06.png | |
exon_skip_491406_SKCM_TCGA-FS-A1Z4-06.png | |
 | Sample: TCGA-KB-A93J-01 |
| Cancer type: STAD | |
| ESID: exon_skip_286384 | |
| Skipped exon start: 7579312 | |
| Skipped exon end: 7579590 | |
| Mutation start: 7579528 | |
| Mutation end: 7579529 | |
| Mutation type: Frame_Shift_Ins | |
| Reference seq: - | |
| Mutation seq: CATT | |
| AAchange: p.W53_F54delinsX | |
| Sample: TCGA-KB-A93J-01 |
| Cancer type: STAD | |
| ESID: exon_skip_286384 | |
| Skipped exon start: 7579312 | |
| Skipped exon end: 7579590 | |
| Mutation start: 7579528 | |
| Mutation end: 7579529 | |
| Mutation type: Frame_Shift_Ins | |
| Reference seq: - | |
| Mutation seq: CATT | |
| AAchange: p.F53fs | |
exon_skip_286384_STAD_TCGA-KB-A93J-01.png | |
exon_skip_78894_STAD_TCGA-KB-A93J-01.png | |
exon_skip_97667_STAD_TCGA-KB-A93J-01.png | |
 | Sample: TCGA-D7-6527-01 |
| Cancer type: STAD | |
| ESID: exon_skip_286384 | |
| Skipped exon start: 7579312 | |
| Skipped exon end: 7579590 | |
| Mutation start: 7579585 | |
| Mutation end: 7579585 | |
| Mutation type: Frame_Shift_Del | |
| Reference seq: G | |
| Mutation seq: - | |
| AAchange: p.L35fs | |
| Sample: TCGA-D7-6527-01 |
| Cancer type: STAD | |
| ESID: exon_skip_286384 | |
| Skipped exon start: 7579312 | |
| Skipped exon end: 7579590 | |
| Mutation start: 7579585 | |
| Mutation end: 7579585 | |
| Mutation type: Frame_Shift_Del | |
| Reference seq: G | |
| Mutation seq: - | |
| AAchange: p.P34fs | |
exon_skip_286384_STAD_TCGA-D7-6527-01.png | |
 | Sample: TCGA-HU-A4HD-01 |
| Cancer type: STAD | |
| ESID: exon_skip_286384 | |
| Skipped exon start: 7579312 | |
| Skipped exon end: 7579590 | |
| Mutation start: 7579470 | |
| Mutation end: 7579471 | |
| Mutation type: Frame_Shift_Ins | |
| Reference seq: - | |
| Mutation seq: G | |
| AAchange: p.V73fs | |
| Sample: TCGA-HU-A4HD-01 |
| Cancer type: STAD | |
| ESID: exon_skip_286384 | |
| Skipped exon start: 7579312 | |
| Skipped exon end: 7579590 | |
| Mutation start: 7579470 | |
| Mutation end: 7579471 | |
| Mutation type: Frame_Shift_Ins | |
| Reference seq: - | |
| Mutation seq: G | |
| AAchange: p.P72fs | |
| Sample: TCGA-HU-A4HD-01 |
| Cancer type: STAD | |
| ESID: exon_skip_286384 | |
| Skipped exon start: 7579312 | |
| Skipped exon end: 7579590 | |
| Mutation start: 7579471 | |
| Mutation end: 7579472 | |
| Mutation type: Frame_Shift_Ins | |
| Reference seq: - | |
| Mutation seq: G | |
| AAchange: p.P72fs | |
exon_skip_286384_STAD_TCGA-HU-A4HD-01.png | |
 | Sample: TCGA-BR-8679-01 |
| Cancer type: STAD | |
| ESID: exon_skip_286384 | |
| Skipped exon start: 7579312 | |
| Skipped exon end: 7579590 | |
| Mutation start: 7579381 | |
| Mutation end: 7579381 | |
| Mutation type: Frame_Shift_Del | |
| Reference seq: G | |
| Mutation seq: - | |
| AAchange: p.Y103fs | |
| Sample: TCGA-BR-8679-01 |
| Cancer type: STAD | |
| ESID: exon_skip_286384 | |
| Skipped exon start: 7579312 | |
| Skipped exon end: 7579590 | |
| Mutation start: 7579381 | |
| Mutation end: 7579381 | |
| Mutation type: Frame_Shift_Del | |
| Reference seq: G | |
| Mutation seq: - | |
| AAchange: p.T102fs | |
exon_skip_286384_STAD_TCGA-BR-8679-01.png | |
 | Sample: TCGA-BR-8486-01 |
| Cancer type: STAD | |
| ESID: exon_skip_286384 | |
| Skipped exon start: 7579312 | |
| Skipped exon end: 7579590 | |
| Mutation start: 7579395 | |
| Mutation end: 7579396 | |
| Mutation type: Frame_Shift_Ins | |
| Reference seq: - | |
| Mutation seq: C | |
| AAchange: p.P98fs | |
| Sample: TCGA-BR-8486-01 |
| Cancer type: STAD | |
| ESID: exon_skip_286384 | |
| Skipped exon start: 7579312 | |
| Skipped exon end: 7579590 | |
| Mutation start: 7579395 | |
| Mutation end: 7579396 | |
| Mutation type: Frame_Shift_Ins | |
| Reference seq: - | |
| Mutation seq: C | |
| AAchange: p.V97fs | |
| Sample: TCGA-BR-8486-01 |
| Cancer type: STAD | |
| ESID: exon_skip_286384 | |
| Skipped exon start: 7579312 | |
| Skipped exon end: 7579590 | |
| Mutation start: 7579396 | |
| Mutation end: 7579397 | |
| Mutation type: Frame_Shift_Ins | |
| Reference seq: - | |
| Mutation seq: C | |
| AAchange: p.V97fs | |
exon_skip_286384_STAD_TCGA-BR-8486-01.png | |
exon_skip_498415_STAD_TCGA-BR-8486-01.png | |
 | Sample: TCGA-HU-8604-01 |
| Cancer type: STAD | |
| ESID: exon_skip_286384 | |
| Skipped exon start: 7579312 | |
| Skipped exon end: 7579590 | |
| Mutation start: 7579585 | |
| Mutation end: 7579585 | |
| Mutation type: Frame_Shift_Del | |
| Reference seq: G | |
| Mutation seq: - | |
| AAchange: p.L35fs | |
exon_skip_286384_STAD_TCGA-HU-8604-01.png | |
 | Sample: TCGA-HU-A4H3-01 |
| Cancer type: STAD | |
| ESID: exon_skip_286384 | |
| Skipped exon start: 7579312 | |
| Skipped exon end: 7579590 | |
| Mutation start: 7579471 | |
| Mutation end: 7579471 | |
| Mutation type: Frame_Shift_Del | |
| Reference seq: G | |
| Mutation seq: - | |
| AAchange: p.V73fs | |
exon_skip_101895_STAD_TCGA-HU-A4H3-01.png | |
exon_skip_101900_STAD_TCGA-HU-A4H3-01.png | |
exon_skip_134053_STAD_TCGA-HU-A4H3-01.png | |
exon_skip_142361_STAD_TCGA-HU-A4H3-01.png | |
exon_skip_21488_STAD_TCGA-HU-A4H3-01.png | |
exon_skip_286384_STAD_TCGA-HU-A4H3-01.png | |
exon_skip_299738_STAD_TCGA-HU-A4H3-01.png | |
exon_skip_307491_STAD_TCGA-HU-A4H3-01.png | |
exon_skip_308974_STAD_TCGA-HU-A4H3-01.png | |
exon_skip_308983_STAD_TCGA-HU-A4H3-01.png | |
exon_skip_312995_STAD_TCGA-HU-A4H3-01.png | |
exon_skip_320688_STAD_TCGA-HU-A4H3-01.png | |
exon_skip_320689_STAD_TCGA-HU-A4H3-01.png | |
exon_skip_320690_STAD_TCGA-HU-A4H3-01.png | |
exon_skip_328488_STAD_TCGA-HU-A4H3-01.png | |
exon_skip_330511_STAD_TCGA-HU-A4H3-01.png | |
exon_skip_450406_STAD_TCGA-HU-A4H3-01.png | |
exon_skip_60290_STAD_TCGA-HU-A4H3-01.png | |
exon_skip_60294_STAD_TCGA-HU-A4H3-01.png | |
exon_skip_69561_STAD_TCGA-HU-A4H3-01.png | |
exon_skip_74347_STAD_TCGA-HU-A4H3-01.png | |
exon_skip_8059_STAD_TCGA-HU-A4H3-01.png | |
 | Sample: TCGA-D1-A17U-01 |
| Cancer type: UCEC | |
| ESID: exon_skip_286384 | |
| Skipped exon start: 7579312 | |
| Skipped exon end: 7579590 | |
| Mutation start: 7579471 | |
| Mutation end: 7579471 | |
| Mutation type: Frame_Shift_Del | |
| Reference seq: G | |
| Mutation seq: - | |
| AAchange: p.P72fs | |
exon_skip_135111_UCEC_TCGA-D1-A17U-01.png | |
exon_skip_135112_UCEC_TCGA-D1-A17U-01.png | |
exon_skip_135114_UCEC_TCGA-D1-A17U-01.png | |
exon_skip_286384_UCEC_TCGA-D1-A17U-01.png | |
exon_skip_294586_UCEC_TCGA-D1-A17U-01.png | |
exon_skip_365789_UCEC_TCGA-D1-A17U-01.png | |
exon_skip_43714_UCEC_TCGA-D1-A17U-01.png | |
 | Sample: TCGA-N5-A4RO-01 |
| Cancer type: UCS | |
| ESID: exon_skip_286384 | |
| Skipped exon start: 7579312 | |
| Skipped exon end: 7579590 | |
| Mutation start: 7579575 | |
| Mutation end: 7579575 | |
| Mutation type: Frame_Shift_Del | |
| Reference seq: G | |
| Mutation seq: - | |
| AAchange: p.Q38fs | |
exon_skip_286384_UCS_TCGA-N5-A4RO-01.png | |
 | Sample: TCGA-09-2044-01 |
| Cancer type: OV | |
| ESID: exon_skip_286379 | |
| Skipped exon start: 7578177 | |
| Skipped exon end: 7578289 | |
| Mutation start: 7578266 | |
| Mutation end: 7578290 | |
| Mutation type: Splice_Site | |
| Reference seq: TAAGATGCTGAGGAGGGGCCAGACC | |
| Mutation seq: - | |
| AAchange: p.G187_splice | |
exon_skip_286379_OV_TCGA-09-2044-01.png | |
 | Sample: TCGA-24-0970-01 |
| Cancer type: OV | |
| ESID: exon_skip_286379 | |
| Skipped exon start: 7578177 | |
| Skipped exon end: 7578289 | |
| Mutation start: 7578290 | |
| Mutation end: 7578290 | |
| Mutation type: Splice_Site | |
| Reference seq: C | |
| Mutation seq: T | |
| AAchange: p.G187_splice | |
exon_skip_286379_OV_TCGA-24-0970-01.png | |
 | Sample: TCGA-N6-A4VG-01 |
| Cancer type: UCS | |
| ESID: exon_skip_286379 | |
| Skipped exon start: 7578177 | |
| Skipped exon end: 7578289 | |
| Mutation start: 7578290 | |
| Mutation end: 7578290 | |
| Mutation type: Splice_Site | |
| Reference seq: C | |
| Mutation seq: T | |
| AAchange: . | |
exon_skip_286379_UCS_TCGA-N6-A4VG-01.png | |
 | Sample: TCGA-LN-A9FO-01 |
| Cancer type: ESCA | |
| ESID: exon_skip_286379 | |
| Skipped exon start: 7578177 | |
| Skipped exon end: 7578289 | |
| Mutation start: 7578239 | |
| Mutation end: 7578239 | |
| Mutation type: Nonsense_Mutation | |
| Reference seq: C | |
| Mutation seq: A | |
| AAchange: p.E204X | |
| Sample: TCGA-LN-A9FO-01 |
| Cancer type: ESCA | |
| ESID: exon_skip_286379 | |
| Skipped exon start: 7578177 | |
| Skipped exon end: 7578289 | |
| Mutation start: 7578239 | |
| Mutation end: 7578239 | |
| Mutation type: Nonsense_Mutation | |
| Reference seq: C | |
| Mutation seq: A | |
| AAchange: p.E204* | |
exon_skip_286379_ESCA_TCGA-LN-A9FO-01.png | |
exon_skip_34463_ESCA_TCGA-LN-A9FO-01.png | |
 | Sample: TCGA-2H-A9GK-01 |
| Cancer type: ESCA | |
| ESID: exon_skip_286379 | |
| Skipped exon start: 7578177 | |
| Skipped exon end: 7578289 | |
| Mutation start: 7578263 | |
| Mutation end: 7578263 | |
| Mutation type: Nonsense_Mutation | |
| Reference seq: G | |
| Mutation seq: A | |
| AAchange: p.R196X | |
| Sample: TCGA-2H-A9GK-01 |
| Cancer type: ESCA | |
| ESID: exon_skip_286379 | |
| Skipped exon start: 7578177 | |
| Skipped exon end: 7578289 | |
| Mutation start: 7578263 | |
| Mutation end: 7578263 | |
| Mutation type: Nonsense_Mutation | |
| Reference seq: G | |
| Mutation seq: A | |
| AAchange: p.R196* | |
exon_skip_112686_ESCA_TCGA-2H-A9GK-01.png | |
exon_skip_286379_ESCA_TCGA-2H-A9GK-01.png | |
 | Sample: TCGA-L5-A4OJ-01 |
| Cancer type: ESCA | |
| ESID: exon_skip_286371 | |
| Skipped exon start: 7576853 | |
| Skipped exon end: 7576926 | |
| Mutation start: 7576921 | |
| Mutation end: 7576925 | |
| Mutation type: Frame_Shift_Del | |
| Reference seq: GCAGT | |
| Mutation seq: - | |
| AAchange: p.308_309del | |
| Sample: TCGA-L5-A4OJ-01 |
| Cancer type: ESCA | |
| ESID: exon_skip_286379 | |
| Skipped exon start: 7578177 | |
| Skipped exon end: 7578289 | |
| Mutation start: 7578257 | |
| Mutation end: 7578257 | |
| Mutation type: Nonsense_Mutation | |
| Reference seq: C | |
| Mutation seq: A | |
| AAchange: p.E198X | |
| Sample: TCGA-L5-A4OJ-01 |
| Cancer type: ESCA | |
| ESID: exon_skip_286379 | |
| Skipped exon start: 7578177 | |
| Skipped exon end: 7578289 | |
| Mutation start: 7578257 | |
| Mutation end: 7578257 | |
| Mutation type: Nonsense_Mutation | |
| Reference seq: C | |
| Mutation seq: A | |
| AAchange: p.E198* | |
exon_skip_151962_ESCA_TCGA-L5-A4OJ-01.png | |
exon_skip_151963_ESCA_TCGA-L5-A4OJ-01.png | |
exon_skip_286379_ESCA_TCGA-L5-A4OJ-01.png | |
exon_skip_325884_ESCA_TCGA-L5-A4OJ-01.png | |
exon_skip_482144_ESCA_TCGA-L5-A4OJ-01.png | |
exon_skip_488311_ESCA_TCGA-L5-A4OJ-01.png | |
exon_skip_77217_ESCA_TCGA-L5-A4OJ-01.png | |
 | Sample: TCGA-CQ-6222-01 |
| Cancer type: HNSC | |
| ESID: exon_skip_286379 | |
| Skipped exon start: 7578177 | |
| Skipped exon end: 7578289 | |
| Mutation start: 7578212 | |
| Mutation end: 7578212 | |
| Mutation type: Nonsense_Mutation | |
| Reference seq: G | |
| Mutation seq: A | |
| AAchange: p.R213* | |
exon_skip_286379_HNSC_TCGA-CQ-6222-01.png | |
 | Sample: TCGA-HW-8319-01 |
| Cancer type: LGG | |
| ESID: exon_skip_286379 | |
| Skipped exon start: 7578177 | |
| Skipped exon end: 7578289 | |
| Mutation start: 7578263 | |
| Mutation end: 7578263 | |
| Mutation type: Nonsense_Mutation | |
| Reference seq: G | |
| Mutation seq: A | |
| AAchange: p.R196X | |
| Sample: TCGA-HW-8319-01 |
| Cancer type: LGG | |
| ESID: exon_skip_286379 | |
| Skipped exon start: 7578177 | |
| Skipped exon end: 7578289 | |
| Mutation start: 7578263 | |
| Mutation end: 7578263 | |
| Mutation type: Nonsense_Mutation | |
| Reference seq: G | |
| Mutation seq: A | |
| AAchange: p.R196* | |
exon_skip_286379_LGG_TCGA-HW-8319-01.png | |
 | Sample: TCGA-44-2666-01 |
| Cancer type: LUAD | |
| ESID: exon_skip_286379 | |
| Skipped exon start: 7578177 | |
| Skipped exon end: 7578289 | |
| Mutation start: 7578263 | |
| Mutation end: 7578263 | |
| Mutation type: Nonsense_Mutation | |
| Reference seq: G | |
| Mutation seq: A | |
| AAchange: p.R196* | |
exon_skip_286379_LUAD_TCGA-44-2666-01.png | |
exon_skip_347690_LUAD_TCGA-44-2666-01.png | |
exon_skip_439050_LUAD_TCGA-44-2666-01.png | |
exon_skip_503611_LUAD_TCGA-44-2666-01.png | |
exon_skip_93891_LUAD_TCGA-44-2666-01.png | |
exon_skip_93913_LUAD_TCGA-44-2666-01.png | |
 | Sample: TCGA-13-0916-01 |
| Cancer type: OV | |
| ESID: exon_skip_286379 | |
| Skipped exon start: 7578177 | |
| Skipped exon end: 7578289 | |
| Mutation start: 7578263 | |
| Mutation end: 7578263 | |
| Mutation type: Nonsense_Mutation | |
| Reference seq: G | |
| Mutation seq: A | |
| AAchange: p.R196* | |
exon_skip_286379_OV_TCGA-13-0916-01.png | |
 | Sample: TCGA-24-1474-01 |
| Cancer type: OV | |
| ESID: exon_skip_286379 | |
| Skipped exon start: 7578177 | |
| Skipped exon end: 7578289 | |
| Mutation start: 7578275 | |
| Mutation end: 7578275 | |
| Mutation type: Nonsense_Mutation | |
| Reference seq: G | |
| Mutation seq: A | |
| AAchange: p.Q192* | |
exon_skip_286379_OV_TCGA-24-1474-01.png | |
 | Sample: TCGA-W3-AA1V-06 |
| Cancer type: SKCM | |
| ESID: exon_skip_286379 | |
| Skipped exon start: 7578177 | |
| Skipped exon end: 7578289 | |
| Mutation start: 7578263 | |
| Mutation end: 7578263 | |
| Mutation type: Nonsense_Mutation | |
| Reference seq: G | |
| Mutation seq: A | |
| AAchange: p.R196* | |
| Sample: TCGA-W3-AA1V-06 |
| Cancer type: SKCM | |
| ESID: exon_skip_286364 | |
| Skipped exon start: 7573927 | |
| Skipped exon end: 7574033 | |
| Mutation start: 7574003 | |
| Mutation end: 7574003 | |
| Mutation type: Nonsense_Mutation | |
| Reference seq: G | |
| Mutation seq: A | |
| AAchange: p.R342* | |
exon_skip_286364_SKCM_TCGA-W3-AA1V-06.png | |
exon_skip_297961_SKCM_TCGA-W3-AA1V-06.png | |
exon_skip_316320_SKCM_TCGA-W3-AA1V-06.png | |
exon_skip_330837_SKCM_TCGA-W3-AA1V-06.png | |
exon_skip_349643_SKCM_TCGA-W3-AA1V-06.png | |
exon_skip_349644_SKCM_TCGA-W3-AA1V-06.png | |
exon_skip_463424_SKCM_TCGA-W3-AA1V-06.png | |
exon_skip_478361_SKCM_TCGA-W3-AA1V-06.png | |
 | Sample: TCGA-VQ-AA68-01 |
| Cancer type: STAD | |
| ESID: exon_skip_286379 | |
| Skipped exon start: 7578177 | |
| Skipped exon end: 7578289 | |
| Mutation start: 7578179 | |
| Mutation end: 7578179 | |
| Mutation type: Nonsense_Mutation | |
| Reference seq: C | |
| Mutation seq: A | |
| AAchange: p.E224X | |
| Sample: TCGA-VQ-AA68-01 |
| Cancer type: STAD | |
| ESID: exon_skip_286379 | |
| Skipped exon start: 7578177 | |
| Skipped exon end: 7578289 | |
| Mutation start: 7578179 | |
| Mutation end: 7578179 | |
| Mutation type: Nonsense_Mutation | |
| Reference seq: C | |
| Mutation seq: A | |
| AAchange: p.E224* | |
exon_skip_286379_STAD_TCGA-VQ-AA68-01.png | |
 | Sample: TCGA-BS-A0UF-01 |
| Cancer type: UCEC | |
| ESID: exon_skip_286379 | |
| Skipped exon start: 7578177 | |
| Skipped exon end: 7578289 | |
| Mutation start: 7578212 | |
| Mutation end: 7578212 | |
| Mutation type: Nonsense_Mutation | |
| Reference seq: G | |
| Mutation seq: A | |
| AAchange: p.R213* | |
exon_skip_104037_UCEC_TCGA-BS-A0UF-01.png | |
exon_skip_105868_UCEC_TCGA-BS-A0UF-01.png | |
exon_skip_105985_UCEC_TCGA-BS-A0UF-01.png | |
exon_skip_115426_UCEC_TCGA-BS-A0UF-01.png | |
exon_skip_14705_UCEC_TCGA-BS-A0UF-01.png | |
exon_skip_147467_UCEC_TCGA-BS-A0UF-01.png | |
exon_skip_19372_UCEC_TCGA-BS-A0UF-01.png | |
exon_skip_286379_UCEC_TCGA-BS-A0UF-01.png | |
exon_skip_294437_UCEC_TCGA-BS-A0UF-01.png | |
exon_skip_321837_UCEC_TCGA-BS-A0UF-01.png | |
exon_skip_324767_UCEC_TCGA-BS-A0UF-01.png | |
exon_skip_345944_UCEC_TCGA-BS-A0UF-01.png | |
exon_skip_345950_UCEC_TCGA-BS-A0UF-01.png | |
exon_skip_382354_UCEC_TCGA-BS-A0UF-01.png | |
exon_skip_389258_UCEC_TCGA-BS-A0UF-01.png | |
exon_skip_389265_UCEC_TCGA-BS-A0UF-01.png | |
exon_skip_39691_UCEC_TCGA-BS-A0UF-01.png | |
exon_skip_40297_UCEC_TCGA-BS-A0UF-01.png | |
exon_skip_461887_UCEC_TCGA-BS-A0UF-01.png | |
exon_skip_482464_UCEC_TCGA-BS-A0UF-01.png | |
exon_skip_59390_UCEC_TCGA-BS-A0UF-01.png | |
exon_skip_82288_UCEC_TCGA-BS-A0UF-01.png | |
exon_skip_84605_UCEC_TCGA-BS-A0UF-01.png | |
exon_skip_95240_UCEC_TCGA-BS-A0UF-01.png | |
 | Sample: TCGA-A2-A0CM-01 |
| Cancer type: BRCA | |
| ESID: exon_skip_286379 | |
| Skipped exon start: 7578177 | |
| Skipped exon end: 7578289 | |
| Mutation start: 7578239 | |
| Mutation end: 7578239 | |
| Mutation type: Frame_Shift_Del | |
| Reference seq: C | |
| Mutation seq: - | |
| AAchange: p.E204fs | |
exon_skip_286379_BRCA_TCGA-A2-A0CM-01.png | |
 | Sample: TCGA-CV-7252-01 |
| Cancer type: HNSC | |
| ESID: exon_skip_286379 | |
| Skipped exon start: 7578177 | |
| Skipped exon end: 7578289 | |
| Mutation start: 7578267 | |
| Mutation end: 7578268 | |
| Mutation type: Frame_Shift_Ins | |
| Reference seq: - | |
| Mutation seq: AG | |
| AAchange: p.H194fs | |
| Sample: TCGA-CV-7252-01 |
| Cancer type: HNSC | |
| ESID: exon_skip_286379 | |
| Skipped exon start: 7578177 | |
| Skipped exon end: 7578289 | |
| Mutation start: 7578267 | |
| Mutation end: 7578268 | |
| Mutation type: Frame_Shift_Ins | |
| Reference seq: - | |
| Mutation seq: AG | |
| AAchange: p.L194fs | |
| Sample: TCGA-CV-7252-01 |
| Cancer type: HNSC | |
| ESID: exon_skip_286384 | |
| Skipped exon start: 7579312 | |
| Skipped exon end: 7579590 | |
| Mutation start: 7579533 | |
| Mutation end: 7579533 | |
| Mutation type: Nonsense_Mutation | |
| Reference seq: G | |
| Mutation seq: A | |
| AAchange: p.Q52* | |
| exon_skip_286384_HNSC_TCGA-CV-7252-01.png | |
 | Sample: TCGA-2J-AABT-01 |
| Cancer type: PAAD | |
| ESID: exon_skip_286379 | |
| Skipped exon start: 7578177 | |
| Skipped exon end: 7578289 | |
| Mutation start: 7578213 | |
| Mutation end: 7578213 | |
| Mutation type: Frame_Shift_Del | |
| Reference seq: A | |
| Mutation seq: - | |
| AAchange: p.F212fs | |
exon_skip_286379_PAAD_TCGA-2J-AABT-01.png | |
 | Sample: TCGA-CG-4477-01 |
| Cancer type: STAD | |
| ESID: exon_skip_286379 | |
| Skipped exon start: 7578177 | |
| Skipped exon end: 7578289 | |
| Mutation start: 7578183 | |
| Mutation end: 7578187 | |
| Mutation type: Frame_Shift_Del | |
| Reference seq: CGGCT | |
| Mutation seq: - | |
| AAchange: p.221_223del | |
| Sample: TCGA-CG-4477-01 |
| Cancer type: STAD | |
| ESID: exon_skip_286379 | |
| Skipped exon start: 7578177 | |
| Skipped exon end: 7578289 | |
| Mutation start: 7578183 | |
| Mutation end: 7578187 | |
| Mutation type: Frame_Shift_Del | |
| Reference seq: CGGCT | |
| Mutation seq: - | |
| AAchange: p.E221fs | |
exon_skip_286379_STAD_TCGA-CG-4477-01.png | |
exon_skip_484749_STAD_TCGA-CG-4477-01.png | |
exon_skip_484750_STAD_TCGA-CG-4477-01.png | |
 | Sample: TCGA-V5-A7RE-01 |
| Cancer type: ESCA | |
| ESID: exon_skip_286376 | |
| Skipped exon start: 7577019 | |
| Skipped exon end: 7577155 | |
| Mutation start: 7577017 | |
| Mutation end: 7577017 | |
| Mutation type: Splice_Site | |
| Reference seq: A | |
| Mutation seq: C | |
| AAchange: . | |
| Sample: TCGA-V5-A7RE-01 |
| Cancer type: ESCA | |
| ESID: exon_skip_286376 | |
| Skipped exon start: 7577019 | |
| Skipped exon end: 7577155 | |
| Mutation start: 7577017 | |
| Mutation end: 7577017 | |
| Mutation type: Splice_Site | |
| Reference seq: A | |
| Mutation seq: C | |
| AAchange: e7+2 | |
exon_skip_286376_ESCA_TCGA-V5-A7RE-01.png | |
exon_skip_391003_ESCA_TCGA-V5-A7RE-01.png | |
exon_skip_391004_ESCA_TCGA-V5-A7RE-01.png | |
 | Sample: TCGA-24-1103-01 |
| Cancer type: OV | |
| ESID: exon_skip_286376 | |
| Skipped exon start: 7577019 | |
| Skipped exon end: 7577155 | |
| Mutation start: 7577018 | |
| Mutation end: 7577018 | |
| Mutation type: Splice_Site | |
| Reference seq: C | |
| Mutation seq: T | |
| AAchange: e7+1 | |
exon_skip_286376_OV_TCGA-24-1103-01.png | |
 | Sample: TCGA-TQ-A7RJ-01 |
| Cancer type: LGG | |
| ESID: exon_skip_286384 | |
| Skipped exon start: 7579312 | |
| Skipped exon end: 7579590 | |
| Mutation start: 7579328 | |
| Mutation end: 7579328 | |
| Mutation type: Frame_Shift_Del | |
| Reference seq: T | |
| Mutation seq: - | |
| AAchange: p.K120fs | |
| Sample: TCGA-TQ-A7RJ-01 |
| Cancer type: LGG | |
| ESID: exon_skip_286376 | |
| Skipped exon start: 7577019 | |
| Skipped exon end: 7577155 | |
| Mutation start: 7577022 | |
| Mutation end: 7577022 | |
| Mutation type: Nonsense_Mutation | |
| Reference seq: G | |
| Mutation seq: A | |
| AAchange: p.R306* | |
| exon_skip_286384_LGG_TCGA-TQ-A7RJ-01.png | |
 | Sample: TCGA-L5-A4OJ-01 |
| Cancer type: ESCA | |
| ESID: exon_skip_286371 | |
| Skipped exon start: 7576853 | |
| Skipped exon end: 7576926 | |
| Mutation start: 7576921 | |
| Mutation end: 7576925 | |
| Mutation type: Frame_Shift_Del | |
| Reference seq: GCAGT | |
| Mutation seq: - | |
| AAchange: p.308_309del | |
| Sample: TCGA-L5-A4OJ-01 |
| Cancer type: ESCA | |
| ESID: exon_skip_286379 | |
| Skipped exon start: 7578177 | |
| Skipped exon end: 7578289 | |
| Mutation start: 7578257 | |
| Mutation end: 7578257 | |
| Mutation type: Nonsense_Mutation | |
| Reference seq: C | |
| Mutation seq: A | |
| AAchange: p.E198X | |
| Sample: TCGA-L5-A4OJ-01 |
| Cancer type: ESCA | |
| ESID: exon_skip_286379 | |
| Skipped exon start: 7578177 | |
| Skipped exon end: 7578289 | |
| Mutation start: 7578257 | |
| Mutation end: 7578257 | |
| Mutation type: Nonsense_Mutation | |
| Reference seq: C | |
| Mutation seq: A | |
| AAchange: p.E198* | |
| exon_skip_151962_ESCA_TCGA-L5-A4OJ-01.png | |
| exon_skip_151963_ESCA_TCGA-L5-A4OJ-01.png | |
| exon_skip_286379_ESCA_TCGA-L5-A4OJ-01.png | |
| exon_skip_325884_ESCA_TCGA-L5-A4OJ-01.png | |
| exon_skip_482144_ESCA_TCGA-L5-A4OJ-01.png | |
| exon_skip_488311_ESCA_TCGA-L5-A4OJ-01.png | |
| exon_skip_77217_ESCA_TCGA-L5-A4OJ-01.png | |
 | Sample: TCGA-63-5128-01 |
| Cancer type: LUSC | |
| ESID: exon_skip_286371 | |
| Skipped exon start: 7576853 | |
| Skipped exon end: 7576926 | |
| Mutation start: 7576878 | |
| Mutation end: 7576887 | |
| Mutation type: Frame_Shift_Del | |
| Reference seq: AGTGGTTTCT | |
| Mutation seq: - | |
| AAchange: p.K320fs | |
exon_skip_286371_LUSC_TCGA-63-5128-01.png | |
exon_skip_517082_LUSC_TCGA-63-5128-01.png | |
 | Sample: TCGA-GR-A4D4-01 |
| Cancer type: DLBC | |
| ESID: exon_skip_286364 | |
| Skipped exon start: 7573927 | |
| Skipped exon end: 7574033 | |
| Mutation start: 7574035 | |
| Mutation end: 7574035 | |
| Mutation type: Splice_Site | |
| Reference seq: T | |
| Mutation seq: C | |
| AAchange: . | |
exon_skip_286364_DLBC_TCGA-GR-A4D4-01.png | |
exon_skip_339532_DLBC_TCGA-GR-A4D4-01.png | |
exon_skip_43768_DLBC_TCGA-GR-A4D4-01.png | |
 | Sample: TCGA-DH-5140-01 |
| Cancer type: LGG | |
| ESID: exon_skip_286364 | |
| Skipped exon start: 7573927 | |
| Skipped exon end: 7574033 | |
| Mutation start: 7574025 | |
| Mutation end: 7574025 | |
| Mutation type: Frame_Shift_Del | |
| Reference seq: C | |
| Mutation seq: - | |
| AAchange: p.R296fs | |
| Sample: TCGA-DH-5140-01 |
| Cancer type: LGG | |
| ESID: exon_skip_286364 | |
| Skipped exon start: 7573927 | |
| Skipped exon end: 7574033 | |
| Mutation start: 7574025 | |
| Mutation end: 7574025 | |
| Mutation type: Frame_Shift_Del | |
| Reference seq: C | |
| Mutation seq: - | |
| AAchange: p.G334fs | |
| Sample: TCGA-DH-5140-01 |
| Cancer type: LGG | |
| ESID: exon_skip_286364 | |
| Skipped exon start: 7573927 | |
| Skipped exon end: 7574033 | |
| Mutation start: 7574035 | |
| Mutation end: 7574035 | |
| Mutation type: Splice_Site | |
| Reference seq: T | |
| Mutation seq: G | |
| AAchange: . | |
exon_skip_286364_LGG_TCGA-DH-5140-01.png | |
 | Sample: TCGA-13-1498-01 |
| Cancer type: OV | |
| ESID: exon_skip_286364 | |
| Skipped exon start: 7573927 | |
| Skipped exon end: 7574033 | |
| Mutation start: 7574034 | |
| Mutation end: 7574034 | |
| Mutation type: Splice_Site | |
| Reference seq: C | |
| Mutation seq: T | |
| AAchange: e9-1 | |
exon_skip_286364_OV_TCGA-13-1498-01.png | |
 | Sample: TCGA-SG-A6Z4-01 |
| Cancer type: SARC | |
| ESID: exon_skip_286364 | |
| Skipped exon start: 7573927 | |
| Skipped exon end: 7574033 | |
| Mutation start: 7574034 | |
| Mutation end: 7574034 | |
| Mutation type: Splice_Site | |
| Reference seq: C | |
| Mutation seq: G | |
| AAchange: e9-1 | |
exon_skip_286364_SARC_TCGA-SG-A6Z4-01.png | |
 | Sample: TCGA-TM-A7CA-01 |
| Cancer type: LGG | |
| ESID: exon_skip_286384 | |
| Skipped exon start: 7579312 | |
| Skipped exon end: 7579590 | |
| Mutation start: 7579420 | |
| Mutation end: 7579420 | |
| Mutation type: Frame_Shift_Del | |
| Reference seq: G | |
| Mutation seq: - | |
| AAchange: p.P89fs | |
| Sample: TCGA-TM-A7CA-01 |
| Cancer type: LGG | |
| ESID: exon_skip_286364 | |
| Skipped exon start: 7573927 | |
| Skipped exon end: 7574033 | |
| Mutation start: 7574003 | |
| Mutation end: 7574003 | |
| Mutation type: Nonsense_Mutation | |
| Reference seq: G | |
| Mutation seq: A | |
| AAchange: p.R342* | |
| exon_skip_286384_LGG_TCGA-TM-A7CA-01.png | |
 | Sample: TCGA-55-8096-01 |
| Cancer type: LUAD | |
| ESID: exon_skip_286364 | |
| Skipped exon start: 7573927 | |
| Skipped exon end: 7574033 | |
| Mutation start: 7574012 | |
| Mutation end: 7574012 | |
| Mutation type: Nonsense_Mutation | |
| Reference seq: C | |
| Mutation seq: A | |
| AAchange: p.E339* | |
exon_skip_105230_LUAD_TCGA-55-8096-01.png | |
exon_skip_286364_LUAD_TCGA-55-8096-01.png | |
 | Sample: TCGA-W3-AA1V-06 |
| Cancer type: SKCM | |
| ESID: exon_skip_286379 | |
| Skipped exon start: 7578177 | |
| Skipped exon end: 7578289 | |
| Mutation start: 7578263 | |
| Mutation end: 7578263 | |
| Mutation type: Nonsense_Mutation | |
| Reference seq: G | |
| Mutation seq: A | |
| AAchange: p.R196* | |
| Sample: TCGA-W3-AA1V-06 |
| Cancer type: SKCM | |
| ESID: exon_skip_286364 | |
| Skipped exon start: 7573927 | |
| Skipped exon end: 7574033 | |
| Mutation start: 7574003 | |
| Mutation end: 7574003 | |
| Mutation type: Nonsense_Mutation | |
| Reference seq: G | |
| Mutation seq: A | |
| AAchange: p.R342* | |
| exon_skip_286364_SKCM_TCGA-W3-AA1V-06.png | |
| exon_skip_297961_SKCM_TCGA-W3-AA1V-06.png | |
| exon_skip_316320_SKCM_TCGA-W3-AA1V-06.png | |
| exon_skip_330837_SKCM_TCGA-W3-AA1V-06.png | |
| exon_skip_349643_SKCM_TCGA-W3-AA1V-06.png | |
| exon_skip_349644_SKCM_TCGA-W3-AA1V-06.png | |
| exon_skip_463424_SKCM_TCGA-W3-AA1V-06.png | |
| exon_skip_478361_SKCM_TCGA-W3-AA1V-06.png | |
 | Sample: TCGA-97-A4M0-01 |
| Cancer type: LUAD | |
| ESID: exon_skip_286364 | |
| Skipped exon start: 7573927 | |
| Skipped exon end: 7574033 | |
| Mutation start: 7574030 | |
| Mutation end: 7574030 | |
| Mutation type: Frame_Shift_Del | |
| Reference seq: G | |
| Mutation seq: - | |
| AAchange: p.R333fs | |
exon_skip_286364_LUAD_TCGA-97-A4M0-01.png | |
| - Non-synonymous mutations located in the skipped exons in CCLE. |
| Sample | Skipped exon start | Skipped exon end | Mutation start | Mutation end | Mutation type | Reference seq | Mutation seq | AAchange |
| EB3_HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 7573927 | 7574033 | 7573990 | 7573993 | Frame_Shift_Del | TCAT | - | p.NE345fs |
| SF539_CENTRAL_NERVOUS_SYSTEM | 7573927 | 7574033 | 7574003 | 7574003 | Frame_Shift_Del | G | - | p.R342fs |
| JHH6_LIVER | 7573927 | 7574033 | 7574009 | 7574019 | Frame_Shift_Del | TCTCGAAGCGC | - | p.ERFEM336fs |
| HCC95_LUNG | 7573927 | 7574033 | 7574025 | 7574025 | Frame_Shift_Del | C | - | p.G334fs |
| NCIH146_LUNG | 7576853 | 7576926 | 7576875 | 7576893 | Frame_Shift_Del | TCCAGTGGTTTCTTCTTTG | - | p.PKKKPLD318fs |
| COV504_OVARY | 7576853 | 7576926 | 7576879 | 7576880 | Frame_Shift_Del | GT | - | p.L323fs |
| EW13_BONE | 7576853 | 7576926 | 7576904 | 7576904 | Frame_Shift_Del | G | - | p.S315fs |
| DND41_HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 7577019 | 7577155 | 7577036 | 7577036 | Frame_Shift_Del | G | - | p.P301fs |
| KCL22_HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 7577019 | 7577155 | 7577036 | 7577036 | Frame_Shift_Del | G | - | p.P301fs |
| LB647SCLC_LUNG | 7577019 | 7577155 | 7577058 | 7577058 | Frame_Shift_Del | C | - | p.E294fs |
| SKMEL30_SKIN | 7577019 | 7577155 | 7577086 | 7577087 | Frame_Shift_Del | TG | - | p.T284fs |
| HCC202_BREAST | 7577019 | 7577155 | 7577086 | 7577087 | Frame_Shift_Del | TG | - | p.T284fs |
| HS633T_SOFT_TISSUE | 7577019 | 7577155 | 7577086 | 7577086 | Frame_Shift_Del | T | - | p.T284fs |
| DMS79_LUNG | 7577019 | 7577155 | 7577101 | 7577101 | Frame_Shift_Del | C | - | p.G279fs |
| NCCIT_TESTIS | 7577019 | 7577155 | 7577124 | 7577124 | Frame_Shift_Del | C | - | p.V272fs |
| TE9_OESOPHAGUS | 7577019 | 7577155 | 7577137 | 7577137 | Frame_Shift_Del | C | - | p.R267fs |
| SNU886_LIVER | 7578177 | 7578289 | 7578192 | 7578193 | Frame_Shift_Del | GG | - | p.P219fs |
| SCC25_UPPER_AERODIGESTIVE_TRACT | 7578177 | 7578289 | 7578222 | 7578223 | Frame_Shift_Del | TC | - | p.R209fs |
| MZ1PC_PANCREAS | 7578177 | 7578289 | 7578222 | 7578223 | Frame_Shift_Del | TC | - | p.R209fs |
| UWB1289_OVARY | 7578177 | 7578289 | 7578222 | 7578223 | Frame_Shift_Del | TC | - | p.R209fs |
| NCIH2882_LUNG | 7578177 | 7578289 | 7578229 | 7578251 | Frame_Shift_Del | TCCAAATACTCCACACGCAAATT | - | p.NLRVEYLD200fs |
| TOLEDO_HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 7578177 | 7578289 | 7578253 | 7578257 | Frame_Shift_Del | CCTTC | - | p.EG198fs |
| TOLEDO_HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 7578177 | 7578289 | 7578253 | 7578259 | Frame_Shift_Del | CCTTCCA | - | p.VEG197fs |
| 59M_OVARY | 7578177 | 7578289 | 7578257 | 7578272 | Frame_Shift_Del | CCACTCGGATAAGATG | - | p.HLIRVE193fs |
| NCIH522_LUNG | 7578177 | 7578289 | 7578277 | 7578277 | Frame_Shift_Del | G | - | p.P191fs |
| SNU1076_UPPER_AERODIGESTIVE_TRACT | 7579312 | 7579590 | 7579319 | 7579329 | Frame_Shift_Del | GTCACAGACTT | - | p.KSVT120fs |
| SNU626_CENTRAL_NERVOUS_SYSTEM | 7579312 | 7579590 | 7579321 | 7579322 | Frame_Shift_Del | CA | - | p.V122fs |
| EW16_BONE | 7579312 | 7579590 | 7579328 | 7579328 | Frame_Shift_Del | T | - | p.K120fs |
| SW948_LARGE_INTESTINE | 7579312 | 7579590 | 7579336 | 7579336 | Frame_Shift_Del | C | - | p.G117fs |
| BHY_UPPER_AERODIGESTIVE_TRACT | 7579312 | 7579590 | 7579336 | 7579336 | Frame_Shift_Del | C | - | p.G117fs |
| BICR22_UPPER_AERODIGESTIVE_TRACT | 7579312 | 7579590 | 7579355 | 7579362 | Frame_Shift_Del | AGACGGAA | - | p.FRL109fs |
| JHU029_UPPER_AERODIGESTIVE_TRACT | 7579312 | 7579590 | 7579364 | 7579364 | Frame_Shift_Del | C | - | p.G108fs |
| OV56_OVARY | 7579312 | 7579590 | 7579383 | 7579384 | Frame_Shift_Del | TT | - | p.KT101fs |
| JHU022_UPPER_AERODIGESTIVE_TRACT | 7579312 | 7579590 | 7579392 | 7579392 | Frame_Shift_Del | A | - | p.S99fs |
| QGP1_PANCREAS | 7579312 | 7579590 | 7579394 | 7579394 | Frame_Shift_Del | G | - | p.P98fs |
| MDAMB157_BREAST | 7579312 | 7579590 | 7579401 | 7579426 | Frame_Shift_Del | AAGATGACAGGGGCCAGGAGGGGGCT | - | p.APSWPLSSS88fs |
| OE21_OESOPHAGUS | 7579312 | 7579590 | 7579417 | 7579417 | Frame_Shift_Del | G | - | p.S90fs |
| L33_PANCREAS | 7579312 | 7579590 | 7579420 | 7579420 | Frame_Shift_Del | G | - | p.P89fs |
| SKOV3_OVARY | 7579312 | 7579590 | 7579420 | 7579420 | Frame_Shift_Del | G | - | p.P89fs |
| AN3CA_ENDOMETRIUM | 7579312 | 7579590 | 7579420 | 7579420 | Frame_Shift_Del | G | - | p.P89fs |
| SNU407_LARGE_INTESTINE | 7579312 | 7579590 | 7579420 | 7579420 | Frame_Shift_Del | G | - | p.P89fs |
| HCC1419_BREAST | 7579312 | 7579590 | 7579461 | 7579467 | Frame_Shift_Del | CAGGGGC | - | p.APA74fs |
| 22RV1_PROSTATE | 7579312 | 7579590 | 7579471 | 7579471 | Frame_Shift_Del | G | - | p.P72fs |
| NCIH2172_LUNG | 7579312 | 7579590 | 7579471 | 7579471 | Frame_Shift_Del | G | - | p.P72fs |
| KM12_LARGE_INTESTINE | 7579312 | 7579590 | 7579471 | 7579471 | Frame_Shift_Del | G | - | p.P72fs |
| RL952_ENDOMETRIUM | 7579312 | 7579590 | 7579471 | 7579471 | Frame_Shift_Del | G | - | p.P72fs |
| OCIMY5_HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 7579312 | 7579590 | 7579471 | 7579471 | Frame_Shift_Del | G | - | p.P72fs |
| JEKO1_HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 7579312 | 7579590 | 7579514 | 7579514 | Frame_Shift_Del | G | - | p.P58fs |
| OACM51_OESOPHAGUS | 7579312 | 7579590 | 7579523 | 7579523 | Frame_Shift_Del | G | - | p.T55fs |
| RVH421_SKIN | 7579312 | 7579590 | 7579533 | 7579533 | Frame_Shift_Del | G | - | p.Q52fs |
| VMRCRCZ_KIDNEY | 7579312 | 7579590 | 7579541 | 7579544 | Frame_Shift_Del | TCGT | - | p.DD48fs |
| NCIH1048_LUNG | 7579312 | 7579590 | 7579547 | 7579547 | Frame_Shift_Del | G | - | p.P47fs |
| ML1_THYROID | 7579312 | 7579590 | 7579547 | 7579547 | Frame_Shift_Del | G | - | p.P47fs |
| LCLC97TM1_LUNG | 7579312 | 7579590 | 7579585 | 7579585 | Frame_Shift_Del | G | - | p.P34fs |
| PACADD188_PANCREAS | 7576853 | 7576926 | 7576868 | 7576869 | Frame_Shift_Ins | - | TC | p.E326fs |
| COLO741_SKIN | 7576853 | 7576926 | 7576882 | 7576883 | Frame_Shift_Ins | - | TT | p.P322fs |
| MEC1_HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 7576853 | 7576926 | 7576896 | 7576897 | Frame_Shift_Ins | - | G | p.Q317fs |
| OE19_OESOPHAGUS | 7576853 | 7576926 | 7576916 | 7576917 | Frame_Shift_Ins | - | T | p.N310fs |
| HSC3_UPPER_AERODIGESTIVE_TRACT | 7577019 | 7577155 | 7577022 | 7577023 | Frame_Shift_Ins | - | CTTA | p.R306fs |
| HO1U1_UPPER_AERODIGESTIVE_TRACT | 7577019 | 7577155 | 7577061 | 7577062 | Frame_Shift_Ins | - | A | p.G293fs |
| EFM192A_BREAST | 7577019 | 7577155 | 7577127 | 7577128 | Frame_Shift_Ins | - | A | p.E271fs |
| SNU478_BILIARY_TRACT | 7577019 | 7577155 | 7577139 | 7577140 | Frame_Shift_Ins | - | A | p.R267fs |
| MDAMB436_BREAST | 7578177 | 7578289 | 7578238 | 7578239 | Frame_Shift_Ins | - | CCACACG | p.E204fs |
| TOLEDO_HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 7578177 | 7578289 | 7578259 | 7578260 | Frame_Shift_Ins | - | GG | p.V197fs |
| A673_BONE | 7579312 | 7579590 | 7579332 | 7579333 | Frame_Shift_Ins | - | TG | p.A119fs |
| IGROV1_OVARY | 7579312 | 7579590 | 7579419 | 7579420 | Frame_Shift_Ins | - | G | p.S90fs |
| HUO3N1_BONE | 7579312 | 7579590 | 7579461 | 7579462 | Frame_Shift_Ins | - | A | p.A76fs |
| CORL303_LUNG | 7579312 | 7579590 | 7579470 | 7579471 | Frame_Shift_Ins | - | G | p.V73fs |
| SNU1040_LARGE_INTESTINE | 7579312 | 7579590 | 7579470 | 7579471 | Frame_Shift_Ins | - | G | p.V73fs |
| SLR25_KIDNEY | 7579312 | 7579590 | 7579470 | 7579471 | Frame_Shift_Ins | - | G | p.V73fs |
| PCI38_UPPER_AERODIGESTIVE_TRACT | 7579312 | 7579590 | 7579546 | 7579547 | Frame_Shift_Ins | - | G | p.P47fs |
| NCIH1339_LUNG | 7579312 | 7579590 | 7579582 | 7579583 | Frame_Shift_Ins | - | A | p.L35fs |
| NCIH1648_LUNG | 7579312 | 7579590 | 7579582 | 7579583 | Frame_Shift_Ins | - | A | p.L35fs |
| PCI4B_UPPER_AERODIGESTIVE_TRACT | 7579700 | 7579721 | 7579709 | 7579710 | Frame_Shift_Ins | - | T | p.N29fs |
| CAL78_BONE | 7577019 | 7577155 | 7577077 | 7577082 | In_Frame_Del | CTCTTC | - | p.EE286del |
| HCC1833_LUNG | 7577019 | 7577155 | 7577080 | 7577088 | In_Frame_Del | TTCCTCTGT | - | p.TEE284del |
| TGW_AUTONOMIC_GANGLIA | 7577019 | 7577155 | 7577090 | 7577092 | In_Frame_Del | CGC | - | p.282_283RR>R |
| HCC827GR5_LUNG | 7578177 | 7578289 | 7578195 | 7578197 | In_Frame_Del | CAC | - | p.V218del |
| LN215_CENTRAL_NERVOUS_SYSTEM | 7578177 | 7578289 | 7578195 | 7578197 | In_Frame_Del | CAC | - | p.V218del |
| HCC827_LUNG | 7578177 | 7578289 | 7578195 | 7578197 | In_Frame_Del | CAC | - | p.V218del |
| RL952_ENDOMETRIUM | 7578177 | 7578289 | 7578195 | 7578197 | In_Frame_Del | CAC | - | p.V218del |
| MHHES1_BONE | 7578177 | 7578289 | 7578204 | 7578206 | In_Frame_Del | ACT | - | p.S215del |
| JHH5_LIVER | 7578177 | 7578289 | 7578269 | 7578280 | In_Frame_Del | GATGCTGAGGAG | - | p.PPQH190del |
| NCIH2818_PLEURA | 7578177 | 7578289 | 7578269 | 7578274 | In_Frame_Del | GATGCT | - | p.QH192del |
| LN215_CENTRAL_NERVOUS_SYSTEM | 7578177 | 7578289 | 7578275 | 7578277 | In_Frame_Del | GAG | - | p.P191del |
| SW1990_PANCREAS | 7578177 | 7578289 | 7578275 | 7578277 | In_Frame_Del | GAG | - | p.P191del |
| DOK_UPPER_AERODIGESTIVE_TRACT | 7578177 | 7578289 | 7578275 | 7578286 | In_Frame_Del | GAGGAGGGGCCA | - | p.LAPP188del |
| PEDS005TPFAD_KIDNEY | 7579312 | 7579590 | 7579347 | 7579367 | In_Frame_Del | AGAAGCCCAGACGGAAACCGT | - | p.YGFRLGF107del |
| HCC1187_BREAST | 7579312 | 7579590 | 7579363 | 7579365 | In_Frame_Del | ACC | - | p.G108del |
| KOSC2_UPPER_AERODIGESTIVE_TRACT | 7579312 | 7579590 | 7579532 | 7579533 | In_Frame_Ins | - | ATG | p.52_52Q>P* |
| SU8686_PANCREAS | 7573927 | 7574033 | 7573948 | 7573948 | Missense_Mutation | C | A | p.G360V |
| MM415_SKIN | 7573927 | 7574033 | 7573986 | 7573987 | Missense_Mutation | GG | AA | p.A347V |
| RMUGS_OVARY | 7573927 | 7574033 | 7573987 | 7573987 | Missense_Mutation | G | A | p.A347V |
| COLO668_LUNG | 7573927 | 7574033 | 7573988 | 7573988 | Missense_Mutation | C | G | p.A347P |
| HEC108_ENDOMETRIUM | 7573927 | 7574033 | 7573993 | 7573993 | Missense_Mutation | T | C | p.N345S |
| KMS12BM_HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 7573927 | 7574033 | 7574017 | 7574017 | Missense_Mutation | C | A | p.R337L |
| LAN2_AUTONOMIC_GANGLIA | 7573927 | 7574033 | 7574018 | 7574018 | Missense_Mutation | G | A | p.R337C |
| KYSE410_OESOPHAGUS | 7573927 | 7574033 | 7574018 | 7574018 | Missense_Mutation | G | A | p.R337C |
| NCIH1184_LUNG | 7573927 | 7574033 | 7574026 | 7574026 | Missense_Mutation | C | A | p.G334V |
| KYSE30_OESOPHAGUS | 7576853 | 7576926 | 7576870 | 7576870 | Missense_Mutation | C | T | p.E326K |
| J82_URINARY_TRACT | 7576853 | 7576926 | 7576886 | 7576886 | Missense_Mutation | C | G | p.K320N |
| SW480_LARGE_INTESTINE | 7576853 | 7576926 | 7576921 | 7576921 | Missense_Mutation | G | A | p.P309S |
| SW620_LARGE_INTESTINE | 7576853 | 7576926 | 7576921 | 7576921 | Missense_Mutation | G | A | p.P309S |
| UBLC1_URINARY_TRACT | 7577019 | 7577155 | 7577052 | 7577052 | Missense_Mutation | G | A | p.H296Y |
| HCC461_LUNG | 7577019 | 7577155 | 7577063 | 7577063 | Missense_Mutation | T | A | p.K292I |
| HCC461_LUNG | 7577019 | 7577155 | 7577066 | 7577067 | Missense_Mutation | TT | AA | p.K291L |
| TE125T_FIBROBLAST | 7577019 | 7577155 | 7577067 | 7577067 | Missense_Mutation | T | C | p.K291E |
| CMLT1_HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 7577019 | 7577155 | 7577070 | 7577070 | Missense_Mutation | G | A | p.R290C |
| JHUEM7_ENDOMETRIUM | 7577019 | 7577155 | 7577077 | 7577077 | Missense_Mutation | C | A | p.E287D |
| LP1_HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 7577019 | 7577155 | 7577082 | 7577082 | Missense_Mutation | C | T | p.E286K |
| M059J_CENTRAL_NERVOUS_SYSTEM | 7577019 | 7577155 | 7577082 | 7577082 | Missense_Mutation | C | T | p.E286K |
| M059K_CENTRAL_NERVOUS_SYSTEM | 7577019 | 7577155 | 7577082 | 7577082 | Missense_Mutation | C | T | p.E286K |
| NCIH3122_LUNG | 7577019 | 7577155 | 7577084 | 7577084 | Missense_Mutation | T | A | p.E285V |
| BT474_BREAST | 7577019 | 7577155 | 7577085 | 7577085 | Missense_Mutation | C | T | p.E285K |
| NCIH1355_LUNG | 7577019 | 7577155 | 7577085 | 7577085 | Missense_Mutation | C | T | p.E285K |
| RPMI8226_HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 7577019 | 7577155 | 7577085 | 7577085 | Missense_Mutation | C | T | p.E285K |
| HT3_CERVIX | 7577019 | 7577155 | 7577085 | 7577085 | Missense_Mutation | C | T | p.E285K |
| NCIH854_LUNG | 7577019 | 7577155 | 7577085 | 7577085 | Missense_Mutation | C | T | p.E285K |
| COLO775_HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 7577019 | 7577155 | 7577085 | 7577085 | Missense_Mutation | C | T | p.E285K |
| NCIH820_LUNG | 7577019 | 7577155 | 7577088 | 7577088 | Missense_Mutation | T | G | p.T284P |
| DG75_HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 7577019 | 7577155 | 7577090 | 7577090 | Missense_Mutation | C | T | p.R283H |
| NCIH64_LUNG | 7577019 | 7577155 | 7577090 | 7577090 | Missense_Mutation | C | G | p.R283P |
| 42MGBA_CENTRAL_NERVOUS_SYSTEM | 7577019 | 7577155 | 7577093 | 7577093 | Missense_Mutation | C | T | p.R282Q |
| LN428_CENTRAL_NERVOUS_SYSTEM | 7577019 | 7577155 | 7577094 | 7577094 | Missense_Mutation | G | A | p.R282W |
| EFE184_ENDOMETRIUM | 7577019 | 7577155 | 7577094 | 7577094 | Missense_Mutation | G | A | p.R282W |
| NCIH510_LUNG | 7577019 | 7577155 | 7577094 | 7577094 | Missense_Mutation | G | C | p.R282G |
| PATU8988T_PANCREAS | 7577019 | 7577155 | 7577094 | 7577094 | Missense_Mutation | G | A | p.R282W |
| CAL29_URINARY_TRACT | 7577019 | 7577155 | 7577094 | 7577094 | Missense_Mutation | G | A | p.R282W |
| HUPT3_PANCREAS | 7577019 | 7577155 | 7577094 | 7577094 | Missense_Mutation | G | A | p.R282W |
| LN405_CENTRAL_NERVOUS_SYSTEM | 7577019 | 7577155 | 7577094 | 7577094 | Missense_Mutation | G | A | p.R282W |
| NB6_AUTONOMIC_GANGLIA | 7577019 | 7577155 | 7577094 | 7577094 | Missense_Mutation | G | A | p.R282W |
| OVKATE_OVARY | 7577019 | 7577155 | 7577094 | 7577094 | Missense_Mutation | G | A | p.R282W |
| PATU8988S_PANCREAS | 7577019 | 7577155 | 7577094 | 7577094 | Missense_Mutation | G | A | p.R282W |
| BALL1_HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 7577019 | 7577155 | 7577096 | 7577096 | Missense_Mutation | T | C | p.D281G |
| SNU201_CENTRAL_NERVOUS_SYSTEM | 7577019 | 7577155 | 7577097 | 7577097 | Missense_Mutation | C | T | p.D281N |
| KURAMOCHI_OVARY | 7577019 | 7577155 | 7577097 | 7577097 | Missense_Mutation | C | A | p.D281Y |
| DOV13_OVARY | 7577019 | 7577155 | 7577098 | 7577098 | Missense_Mutation | T | A | p.R280S |
| RH30_SOFT_TISSUE | 7577019 | 7577155 | 7577098 | 7577098 | Missense_Mutation | T | A | p.R280S |
| HS294T_SKIN | 7577019 | 7577155 | 7577098 | 7577098 | Missense_Mutation | T | A | p.R280S |
| SJRH30_SOFT_TISSUE | 7577019 | 7577155 | 7577098 | 7577098 | Missense_Mutation | T | A | p.R280S |
| UMUC14_URINARY_TRACT | 7577019 | 7577155 | 7577099 | 7577099 | Missense_Mutation | C | G | p.R280T |
| JMSU1_URINARY_TRACT | 7577019 | 7577155 | 7577099 | 7577099 | Missense_Mutation | C | G | p.R280T |
| KMBC2_URINARY_TRACT | 7577019 | 7577155 | 7577099 | 7577099 | Missense_Mutation | C | G | p.R280T |
| 5637_URINARY_TRACT | 7577019 | 7577155 | 7577099 | 7577099 | Missense_Mutation | C | G | p.R280T |
| CAMA1_BREAST | 7577019 | 7577155 | 7577099 | 7577099 | Missense_Mutation | C | G | p.R280T |
| MDAMB231_BREAST | 7577019 | 7577155 | 7577099 | 7577099 | Missense_Mutation | C | T | p.R280K |
| MLMA_HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 7577019 | 7577155 | 7577100 | 7577100 | Missense_Mutation | T | C | p.R280G |
| CJM_SKIN | 7577019 | 7577155 | 7577100 | 7577100 | Missense_Mutation | T | C | p.R280G |
| SCLC22H_LUNG | 7577019 | 7577155 | 7577105 | 7577105 | Missense_Mutation | G | C | p.P278R |
| WM983B_SKIN | 7577019 | 7577155 | 7577105 | 7577106 | Missense_Mutation | GG | AA | p.P278F |
| SCLC21H_LUNG | 7577019 | 7577155 | 7577105 | 7577105 | Missense_Mutation | G | C | p.P278R |
| CCK81_LARGE_INTESTINE | 7577019 | 7577155 | 7577105 | 7577105 | Missense_Mutation | G | T | p.P278H |
| LU134A_LUNG | 7577019 | 7577155 | 7577105 | 7577105 | Missense_Mutation | G | A | p.P278L |
| NB7_AUTONOMIC_GANGLIA | 7577019 | 7577155 | 7577105 | 7577105 | Missense_Mutation | G | A | p.P278L |
| RERFLCAD1_LUNG | 7577019 | 7577155 | 7577105 | 7577105 | Missense_Mutation | G | A | p.P278L |
| WM983B_SKIN | 7577019 | 7577155 | 7577105 | 7577105 | Missense_Mutation | G | A | p.P278L |
| RERFLCAD1_LUNG | 7577019 | 7577155 | 7577105 | 7577106 | Missense_Mutation | GG | AA | p.P278F |
| MCC13_SKIN | 7577019 | 7577155 | 7577106 | 7577106 | Missense_Mutation | G | A | p.P278S |
| HS839T_FIBROBLAST | 7577019 | 7577155 | 7577106 | 7577106 | Missense_Mutation | G | A | p.P278S |
| MKN7_STOMACH | 7577019 | 7577155 | 7577106 | 7577106 | Missense_Mutation | G | A | p.P278S |
| ABC1_LUNG | 7577019 | 7577155 | 7577106 | 7577106 | Missense_Mutation | G | A | p.P278S |
| 786O_KIDNEY | 7577019 | 7577155 | 7577106 | 7577106 | Missense_Mutation | G | C | p.P278A |
| RERFLCAD1_LUNG | 7577019 | 7577155 | 7577106 | 7577106 | Missense_Mutation | G | A | p.P278S |
| WM983B_SKIN | 7577019 | 7577155 | 7577106 | 7577106 | Missense_Mutation | G | A | p.P278S |
| FLO1_OESOPHAGUS | 7577019 | 7577155 | 7577108 | 7577108 | Missense_Mutation | C | A | p.C277F |
| G401_SOFT_TISSUE | 7577019 | 7577155 | 7577108 | 7577108 | Missense_Mutation | C | A | p.C277F |
| SW1271_LUNG | 7577019 | 7577155 | 7577108 | 7577108 | Missense_Mutation | C | A | p.C277F |
| NCIH2135_LUNG | 7577019 | 7577155 | 7577108 | 7577108 | Missense_Mutation | C | A | p.C277F |
| NCIH250_LUNG | 7577019 | 7577155 | 7577108 | 7577108 | Missense_Mutation | C | A | p.C277F |
| CHAGOK1_LUNG | 7577019 | 7577155 | 7577114 | 7577114 | Missense_Mutation | C | A | p.C275F |
| GI1_CENTRAL_NERVOUS_SYSTEM | 7577019 | 7577155 | 7577114 | 7577114 | Missense_Mutation | C | T | p.C275Y |
| JHOM2B_OVARY | 7577019 | 7577155 | 7577114 | 7577114 | Missense_Mutation | C | A | p.C275F |
| PFSK1_CENTRAL_NERVOUS_SYSTEM | 7577019 | 7577155 | 7577115 | 7577115 | Missense_Mutation | A | C | p.C275G |
| D425_CENTRAL_NERVOUS_SYSTEM | 7577019 | 7577155 | 7577117 | 7577118 | Missense_Mutation | AC | CA | p.V274C |
| DU145_PROSTATE | 7577019 | 7577155 | 7577118 | 7577118 | Missense_Mutation | C | A | p.V274F |
| A2058_SKIN | 7577019 | 7577155 | 7577118 | 7577118 | Missense_Mutation | C | A | p.V274F |
| A431_SKIN | 7577019 | 7577155 | 7577120 | 7577120 | Missense_Mutation | C | T | p.R273H |
| COGE352_BONE | 7577019 | 7577155 | 7577120 | 7577120 | Missense_Mutation | C | T | p.R273H |
| EGI1_BILIARY_TRACT | 7577019 | 7577155 | 7577120 | 7577120 | Missense_Mutation | C | T | p.R273H |
| MONOMAC1_HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 7577019 | 7577155 | 7577120 | 7577120 | Missense_Mutation | C | T | p.R273H |
| OC316_OVARY | 7577019 | 7577155 | 7577120 | 7577120 | Missense_Mutation | C | T | p.R273H |
| PF382_HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 7577019 | 7577155 | 7577120 | 7577121 | Missense_Mutation | CG | TA | p.R273Y |
| R262_CENTRAL_NERVOUS_SYSTEM | 7577019 | 7577155 | 7577120 | 7577120 | Missense_Mutation | C | T | p.R273H |
| SF268_CENTRAL_NERVOUS_SYSTEM | 7577019 | 7577155 | 7577120 | 7577120 | Missense_Mutation | C | T | p.R273H |
| FTC238_THYROID | 7577019 | 7577155 | 7577120 | 7577120 | Missense_Mutation | C | T | p.R273H |
| HEC59_ENDOMETRIUM | 7577019 | 7577155 | 7577120 | 7577120 | Missense_Mutation | C | T | p.R273H |
| HEC6_ENDOMETRIUM | 7577019 | 7577155 | 7577120 | 7577120 | Missense_Mutation | C | T | p.R273H |
| HT_HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 7577019 | 7577155 | 7577120 | 7577120 | Missense_Mutation | C | T | p.R273H |
| SNU503_LARGE_INTESTINE | 7577019 | 7577155 | 7577120 | 7577120 | Missense_Mutation | C | A | p.R273L |
| SNU601_STOMACH | 7577019 | 7577155 | 7577120 | 7577120 | Missense_Mutation | C | T | p.R273H |
| SNUC2A_LARGE_INTESTINE | 7577019 | 7577155 | 7577120 | 7577121 | Missense_Mutation | CG | TA | p.R273Y |
| YD8_UPPER_AERODIGESTIVE_TRACT | 7577019 | 7577155 | 7577120 | 7577120 | Missense_Mutation | C | T | p.R273H |
| HT29_LARGE_INTESTINE | 7577019 | 7577155 | 7577120 | 7577120 | Missense_Mutation | C | T | p.R273H |
| NCIH1876_LUNG | 7577019 | 7577155 | 7577120 | 7577120 | Missense_Mutation | C | A | p.R273L |
| SKMEL30_SKIN | 7577019 | 7577155 | 7577120 | 7577120 | Missense_Mutation | C | T | p.R273H |
| SW480_LARGE_INTESTINE | 7577019 | 7577155 | 7577120 | 7577120 | Missense_Mutation | C | T | p.R273H |
| HCC38_BREAST | 7577019 | 7577155 | 7577120 | 7577120 | Missense_Mutation | C | A | p.R273L |
| NCIH1793_LUNG | 7577019 | 7577155 | 7577120 | 7577120 | Missense_Mutation | C | T | p.R273H |
| NCIH1975_LUNG | 7577019 | 7577155 | 7577120 | 7577120 | Missense_Mutation | C | T | p.R273H |
| NCIH508_LARGE_INTESTINE | 7577019 | 7577155 | 7577120 | 7577120 | Missense_Mutation | C | T | p.R273H |
| PANC1_PANCREAS | 7577019 | 7577155 | 7577120 | 7577120 | Missense_Mutation | C | T | p.R273H |
| SNUC2A_LARGE_INTESTINE | 7577019 | 7577155 | 7577120 | 7577120 | Missense_Mutation | C | T | p.R273H |
| SUIT2_PANCREAS | 7577019 | 7577155 | 7577120 | 7577120 | Missense_Mutation | C | T | p.R273H |
| SW1783_CENTRAL_NERVOUS_SYSTEM | 7577019 | 7577155 | 7577120 | 7577120 | Missense_Mutation | C | T | p.R273H |
| U251MG_CENTRAL_NERVOUS_SYSTEM | 7577019 | 7577155 | 7577120 | 7577120 | Missense_Mutation | C | T | p.R273H |
| ARH77_HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 7577019 | 7577155 | 7577120 | 7577120 | Missense_Mutation | C | T | p.R273H |
| ECGI10_OESOPHAGUS | 7577019 | 7577155 | 7577120 | 7577120 | Missense_Mutation | C | A | p.R273L |
| EN_ENDOMETRIUM | 7577019 | 7577155 | 7577120 | 7577120 | Missense_Mutation | C | T | p.R273H |
| FTC133_THYROID | 7577019 | 7577155 | 7577120 | 7577120 | Missense_Mutation | C | T | p.R273H |
| NCIH2810_PLEURA | 7577019 | 7577155 | 7577120 | 7577120 | Missense_Mutation | C | A | p.R273L |
| KP1N_PANCREAS | 7577019 | 7577155 | 7577120 | 7577120 | Missense_Mutation | C | T | p.R273H |
| MDAMB468_BREAST | 7577019 | 7577155 | 7577120 | 7577120 | Missense_Mutation | C | T | p.R273H |
| MOLT13_HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 7577019 | 7577155 | 7577120 | 7577120 | Missense_Mutation | C | T | p.R273H |
| MONOMAC6_HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 7577019 | 7577155 | 7577120 | 7577120 | Missense_Mutation | C | T | p.R273H |
| NCIH1155_LUNG | 7577019 | 7577155 | 7577120 | 7577120 | Missense_Mutation | C | T | p.R273H |
| NCIH1623_LUNG | 7577019 | 7577155 | 7577120 | 7577120 | Missense_Mutation | C | A | p.R273L |
| NCIH1734_LUNG | 7577019 | 7577155 | 7577120 | 7577120 | Missense_Mutation | C | A | p.R273L |
| NCIH1838_LUNG | 7577019 | 7577155 | 7577120 | 7577120 | Missense_Mutation | C | A | p.R273L |
| NCIH2009_LUNG | 7577019 | 7577155 | 7577120 | 7577120 | Missense_Mutation | C | A | p.R273L |
| NCIH2405_LUNG | 7577019 | 7577155 | 7577120 | 7577120 | Missense_Mutation | C | T | p.R273H |
| NOS1_BONE | 7577019 | 7577155 | 7577120 | 7577120 | Missense_Mutation | C | T | p.R273H |
| OC314_OVARY | 7577019 | 7577155 | 7577120 | 7577120 | Missense_Mutation | C | T | p.R273H |
| OVCA420_OVARY | 7577019 | 7577155 | 7577120 | 7577120 | Missense_Mutation | C | T | p.R273H |
| PF382_HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 7577019 | 7577155 | 7577120 | 7577120 | Missense_Mutation | C | T | p.R273H |
| SKGIIIA_CERVIX | 7577019 | 7577155 | 7577120 | 7577120 | Missense_Mutation | C | T | p.R273H |
| SUDHL1_HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 7577019 | 7577155 | 7577120 | 7577120 | Missense_Mutation | C | T | p.R273H |
| SUPT1_HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 7577019 | 7577155 | 7577120 | 7577120 | Missense_Mutation | C | T | p.R273H |
| SW620_LARGE_INTESTINE | 7577019 | 7577155 | 7577120 | 7577120 | Missense_Mutation | C | T | p.R273H |
| SJSA1_BONE | 7577019 | 7577155 | 7577120 | 7577120 | Missense_Mutation | C | T | p.R273H |
| SNUC2B_LARGE_INTESTINE | 7577019 | 7577155 | 7577120 | 7577121 | Missense_Mutation | CG | TA | p.R273Y |
| SW1783_CENTRAL_NERVOUS_SYSTEM | 7577019 | 7577155 | 7577120 | 7577121 | Missense_Mutation | CG | TA | p.R273Y |
| KP1NL_PANCREAS | 7577019 | 7577155 | 7577120 | 7577120 | Missense_Mutation | C | T | p.R273H |
| C33A_CERVIX | 7577019 | 7577155 | 7577121 | 7577121 | Missense_Mutation | G | A | p.R273C |
| NCIH1048_LUNG | 7577019 | 7577155 | 7577121 | 7577121 | Missense_Mutation | G | A | p.R273C |
| RDES_BONE | 7577019 | 7577155 | 7577121 | 7577121 | Missense_Mutation | G | A | p.R273C |
| RH30_SOFT_TISSUE | 7577019 | 7577155 | 7577121 | 7577121 | Missense_Mutation | G | A | p.R273C |
| SUM229PE_BREAST | 7577019 | 7577155 | 7577121 | 7577121 | Missense_Mutation | G | A | p.R273C |
| YAMATO_SOFT_TISSUE | 7577019 | 7577155 | 7577121 | 7577121 | Missense_Mutation | G | A | p.R273C |
| BL70_HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 7577019 | 7577155 | 7577121 | 7577121 | Missense_Mutation | G | A | p.R273C |
| CL14_LARGE_INTESTINE | 7577019 | 7577155 | 7577121 | 7577121 | Missense_Mutation | G | A | p.R273C |
| PANC0213_PANCREAS | 7577019 | 7577155 | 7577121 | 7577121 | Missense_Mutation | G | A | p.R273C |
| RPMI8402_HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 7577019 | 7577155 | 7577121 | 7577121 | Missense_Mutation | G | A | p.R273C |
| SH10TC_STOMACH | 7577019 | 7577155 | 7577121 | 7577121 | Missense_Mutation | G | A | p.R273C |
| SNU1196_BILIARY_TRACT | 7577019 | 7577155 | 7577121 | 7577121 | Missense_Mutation | G | A | p.R273C |
| SUDHL4_HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 7577019 | 7577155 | 7577121 | 7577121 | Missense_Mutation | G | A | p.R273C |
| EFO27_OVARY | 7577019 | 7577155 | 7577121 | 7577121 | Missense_Mutation | G | A | p.R273C |
| 8305C_THYROID | 7577019 | 7577155 | 7577121 | 7577121 | Missense_Mutation | G | A | p.R273C |
| KARPAS299_HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 7577019 | 7577155 | 7577121 | 7577121 | Missense_Mutation | G | A | p.R273C |
| MFE319_ENDOMETRIUM | 7577019 | 7577155 | 7577121 | 7577121 | Missense_Mutation | G | A | p.R273C |
| SNUC2A_LARGE_INTESTINE | 7577019 | 7577155 | 7577121 | 7577121 | Missense_Mutation | G | A | p.R273C |
| SW1783_CENTRAL_NERVOUS_SYSTEM | 7577019 | 7577155 | 7577121 | 7577121 | Missense_Mutation | G | A | p.R273C |
| 8MGBA_CENTRAL_NERVOUS_SYSTEM | 7577019 | 7577155 | 7577121 | 7577121 | Missense_Mutation | G | A | p.R273C |
| CHSA0108_BONE | 7577019 | 7577155 | 7577121 | 7577121 | Missense_Mutation | G | A | p.R273C |
| EW11_BONE | 7577019 | 7577155 | 7577121 | 7577121 | Missense_Mutation | G | A | p.R273C |
| EW12_BONE | 7577019 | 7577155 | 7577121 | 7577121 | Missense_Mutation | G | A | p.R273C |
| EW1_BONE | 7577019 | 7577155 | 7577121 | 7577121 | Missense_Mutation | G | A | p.R273C |
| NCIH2595_PLEURA | 7577019 | 7577155 | 7577121 | 7577121 | Missense_Mutation | G | A | p.R273C |
| KARPAS45_HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 7577019 | 7577155 | 7577121 | 7577121 | Missense_Mutation | G | A | p.R273C |
| NO11_CENTRAL_NERVOUS_SYSTEM | 7577019 | 7577155 | 7577121 | 7577121 | Missense_Mutation | G | A | p.R273C |
| PCI15A_UPPER_AERODIGESTIVE_TRACT | 7577019 | 7577155 | 7577121 | 7577121 | Missense_Mutation | G | A | p.R273C |
| PF382_HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 7577019 | 7577155 | 7577121 | 7577121 | Missense_Mutation | G | A | p.R273C |
| SJRH30_SOFT_TISSUE | 7577019 | 7577155 | 7577121 | 7577121 | Missense_Mutation | G | A | p.R273C |
| SW1088_CENTRAL_NERVOUS_SYSTEM | 7577019 | 7577155 | 7577121 | 7577121 | Missense_Mutation | G | A | p.R273C |
| SW1710_URINARY_TRACT | 7577019 | 7577155 | 7577121 | 7577121 | Missense_Mutation | G | A | p.R273C |
| TASK1_CENTRAL_NERVOUS_SYSTEM | 7577019 | 7577155 | 7577121 | 7577121 | Missense_Mutation | G | A | p.R273C |
| TGBC11TKB_STOMACH | 7577019 | 7577155 | 7577121 | 7577121 | Missense_Mutation | G | A | p.R273C |
| TT2609C02_THYROID | 7577019 | 7577155 | 7577121 | 7577121 | Missense_Mutation | G | A | p.R273C |
| MCC142_SKIN | 7577019 | 7577155 | 7577123 | 7577123 | Missense_Mutation | A | T | p.V272E |
| CHLA99_BONE | 7577019 | 7577155 | 7577124 | 7577124 | Missense_Mutation | C | A | p.V272L |
| GSU_STOMACH | 7577019 | 7577155 | 7577124 | 7577124 | Missense_Mutation | C | T | p.V272M |
| KE39_STOMACH | 7577019 | 7577155 | 7577124 | 7577124 | Missense_Mutation | C | A | p.V272L |
| TE5_OESOPHAGUS | 7577019 | 7577155 | 7577124 | 7577124 | Missense_Mutation | C | A | p.V272L |
| LK2_LUNG | 7577019 | 7577155 | 7577124 | 7577124 | Missense_Mutation | C | T | p.V272M |
| TE1_OESOPHAGUS | 7577019 | 7577155 | 7577124 | 7577124 | Missense_Mutation | C | T | p.V272M |
| ATN1_HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 7577019 | 7577155 | 7577124 | 7577124 | Missense_Mutation | C | G | p.V272L |
| CAR1_LARGE_INTESTINE | 7577019 | 7577155 | 7577124 | 7577124 | Missense_Mutation | C | T | p.V272M |
| KMOE2_HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 7577019 | 7577155 | 7577124 | 7577124 | Missense_Mutation | C | T | p.V272M |
| LOUCY_HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 7577019 | 7577155 | 7577124 | 7577124 | Missense_Mutation | C | T | p.V272M |
| HUH28_BILIARY_TRACT | 7577019 | 7577155 | 7577127 | 7577127 | Missense_Mutation | C | T | p.E271K |
| J82_URINARY_TRACT | 7577019 | 7577155 | 7577127 | 7577127 | Missense_Mutation | C | T | p.E271K |
| U178_CENTRAL_NERVOUS_SYSTEM | 7577019 | 7577155 | 7577127 | 7577127 | Missense_Mutation | C | T | p.E271K |
| HMVII_SKIN | 7577019 | 7577155 | 7577135 | 7577135 | Missense_Mutation | T | A | p.N268I |
| HCC2429_LUNG | 7577019 | 7577155 | 7577138 | 7577138 | Missense_Mutation | C | T | p.R267Q |
| NCIH1437_LUNG | 7577019 | 7577155 | 7577138 | 7577138 | Missense_Mutation | C | G | p.R267P |
| JHH7_LIVER | 7577019 | 7577155 | 7577138 | 7577138 | Missense_Mutation | C | G | p.R267P |
| NCIH740_LUNG | 7577019 | 7577155 | 7577138 | 7577138 | Missense_Mutation | C | G | p.R267P |
| SUPT1_HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 7577019 | 7577155 | 7577138 | 7577138 | Missense_Mutation | C | A | p.R267L |
| HCC461_LUNG | 7577019 | 7577155 | 7577138 | 7577138 | Missense_Mutation | C | T | p.R267Q |
| PL18_PANCREAS | 7577019 | 7577155 | 7577139 | 7577139 | Missense_Mutation | G | A | p.R267W |
| SKMEL3_SKIN | 7577019 | 7577155 | 7577139 | 7577139 | Missense_Mutation | G | A | p.R267W |
| DJM1_SKIN | 7577019 | 7577155 | 7577141 | 7577141 | Missense_Mutation | C | A | p.G266V |
| M14_SKIN | 7577019 | 7577155 | 7577141 | 7577141 | Missense_Mutation | C | T | p.G266E |
| PL4_PANCREAS | 7577019 | 7577155 | 7577141 | 7577141 | Missense_Mutation | C | A | p.G266V |
| SW962_VULVA | 7577019 | 7577155 | 7577141 | 7577141 | Missense_Mutation | C | A | p.G266V |
| DAUDI_HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 7577019 | 7577155 | 7577141 | 7577141 | Missense_Mutation | C | T | p.G266E |
| JHESOAD1_OESOPHAGUS | 7577019 | 7577155 | 7577141 | 7577141 | Missense_Mutation | C | T | p.G266E |
| MDAMB435S_SKIN | 7577019 | 7577155 | 7577141 | 7577141 | Missense_Mutation | C | T | p.G266E |
| NCO2_HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 7577019 | 7577155 | 7577142 | 7577142 | Missense_Mutation | C | G | p.G266R |
| HO1N1_UPPER_AERODIGESTIVE_TRACT | 7577019 | 7577155 | 7577142 | 7577142 | Missense_Mutation | C | G | p.G266R |
| GAMG_CENTRAL_NERVOUS_SYSTEM | 7577019 | 7577155 | 7577144 | 7577144 | Missense_Mutation | A | G | p.L265P |
| TK10_KIDNEY | 7577019 | 7577155 | 7577147 | 7577147 | Missense_Mutation | A | C | p.L264R |
| SW626_OVARY | 7577019 | 7577155 | 7577153 | 7577153 | Missense_Mutation | C | A | p.G262V |
| SNU475_LIVER | 7577019 | 7577155 | 7577153 | 7577153 | Missense_Mutation | C | T | p.G262D |
| NCIH2030_LUNG | 7577019 | 7577155 | 7577153 | 7577153 | Missense_Mutation | C | A | p.G262V |
| CAL148_BREAST | 7578177 | 7578289 | 7578179 | 7578179 | Missense_Mutation | C | T | p.E224K |
| DU145_PROSTATE | 7578177 | 7578289 | 7578181 | 7578181 | Missense_Mutation | G | A | p.P223L |
| RO82W1_THYROID | 7578177 | 7578289 | 7578181 | 7578181 | Missense_Mutation | G | A | p.P223L |
| EW8_BONE | 7578177 | 7578289 | 7578190 | 7578190 | Missense_Mutation | T | C | p.Y220C |
| HCC2935_LUNG | 7578177 | 7578289 | 7578190 | 7578190 | Missense_Mutation | T | C | p.Y220C |
| HCC366_LUNG | 7578177 | 7578289 | 7578190 | 7578190 | Missense_Mutation | T | C | p.Y220C |
| MFE296_ENDOMETRIUM | 7578177 | 7578289 | 7578190 | 7578190 | Missense_Mutation | T | C | p.Y220C |
| T3M4_PANCREAS | 7578177 | 7578289 | 7578190 | 7578190 | Missense_Mutation | T | C | p.Y220C |
| NUGC3_STOMACH | 7578177 | 7578289 | 7578190 | 7578190 | Missense_Mutation | T | C | p.Y220C |
| COV362_OVARY | 7578177 | 7578289 | 7578190 | 7578190 | Missense_Mutation | T | C | p.Y220C |
| HCC1419_BREAST | 7578177 | 7578289 | 7578190 | 7578190 | Missense_Mutation | T | C | p.Y220C |
| MFE319_ENDOMETRIUM | 7578177 | 7578289 | 7578190 | 7578190 | Missense_Mutation | T | C | p.Y220C |
| 451LU_SKIN | 7578177 | 7578289 | 7578190 | 7578190 | Missense_Mutation | T | C | p.Y220C |
| BXPC3_PANCREAS | 7578177 | 7578289 | 7578190 | 7578190 | Missense_Mutation | T | C | p.Y220C |
| HUH7_LIVER | 7578177 | 7578289 | 7578190 | 7578190 | Missense_Mutation | T | C | p.Y220C |
| KON_UPPER_AERODIGESTIVE_TRACT | 7578177 | 7578289 | 7578190 | 7578190 | Missense_Mutation | T | C | p.Y220C |
| MDAMB330_BREAST | 7578177 | 7578289 | 7578190 | 7578190 | Missense_Mutation | T | C | p.Y220C |
| NCIH2085_LUNG | 7578177 | 7578289 | 7578190 | 7578190 | Missense_Mutation | T | C | p.Y220C |
| NCIH2342_LUNG | 7578177 | 7578289 | 7578190 | 7578190 | Missense_Mutation | T | C | p.Y220C |
| NCIH748_LUNG | 7578177 | 7578289 | 7578190 | 7578190 | Missense_Mutation | T | C | p.Y220C |
| RH1_SOFT_TISSUE | 7578177 | 7578289 | 7578190 | 7578190 | Missense_Mutation | T | C | p.Y220C |
| U698M_HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 7578177 | 7578289 | 7578190 | 7578190 | Missense_Mutation | T | C | p.Y220C |
| TE8_OESOPHAGUS | 7578177 | 7578289 | 7578190 | 7578190 | Missense_Mutation | T | C | p.Y220C |
| FU97_STOMACH | 7578177 | 7578289 | 7578191 | 7578191 | Missense_Mutation | A | C | p.Y220D |
| NCIH2029_LUNG | 7578177 | 7578289 | 7578191 | 7578191 | Missense_Mutation | A | C | p.Y220D |
| SNUC5_LARGE_INTESTINE | 7578177 | 7578289 | 7578197 | 7578197 | Missense_Mutation | C | A | p.V218L |
| SNU308_BILIARY_TRACT | 7578177 | 7578289 | 7578199 | 7578199 | Missense_Mutation | A | C | p.V217G |
| OV17R_OVARY | 7578177 | 7578289 | 7578203 | 7578203 | Missense_Mutation | C | T | p.V216M |
| HT_HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 7578177 | 7578289 | 7578203 | 7578203 | Missense_Mutation | C | T | p.V216M |
| SNU216_STOMACH | 7578177 | 7578289 | 7578203 | 7578203 | Missense_Mutation | C | T | p.V216M |
| ECC12_STOMACH | 7578177 | 7578289 | 7578203 | 7578203 | Missense_Mutation | C | T | p.V216M |
| HS940T_FIBROBLAST | 7578177 | 7578289 | 7578203 | 7578203 | Missense_Mutation | C | A | p.V216L |
| LCLC103H_LUNG | 7578177 | 7578289 | 7578203 | 7578203 | Missense_Mutation | C | A | p.V216L |
| CL11_LARGE_INTESTINE | 7578177 | 7578289 | 7578205 | 7578205 | Missense_Mutation | C | T | p.S215N |
| SNU213_PANCREAS | 7578177 | 7578289 | 7578205 | 7578205 | Missense_Mutation | C | A | p.S215I |
| SNU668_STOMACH | 7578177 | 7578289 | 7578205 | 7578205 | Missense_Mutation | C | T | p.S215N |
| NCIH661_LUNG | 7578177 | 7578289 | 7578205 | 7578205 | Missense_Mutation | C | A | p.S215I |
| SNU182_LIVER | 7578177 | 7578289 | 7578205 | 7578205 | Missense_Mutation | C | A | p.S215I |
| BC3C_URINARY_TRACT | 7578177 | 7578289 | 7578205 | 7578205 | Missense_Mutation | C | T | p.S215N |
| MTA_HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 7578177 | 7578289 | 7578206 | 7578206 | Missense_Mutation | T | C | p.S215G |
| OV90_OVARY | 7578177 | 7578289 | 7578206 | 7578206 | Missense_Mutation | T | G | p.S215R |
| DEL_HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 7578177 | 7578289 | 7578206 | 7578206 | Missense_Mutation | T | A | p.S215C |
| NCIH1963_LUNG | 7578177 | 7578289 | 7578208 | 7578208 | Missense_Mutation | T | C | p.H214R |
| TT_OESOPHAGUS | 7578177 | 7578289 | 7578208 | 7578208 | Missense_Mutation | T | C | p.H214R |
| LN443_CENTRAL_NERVOUS_SYSTEM | 7578177 | 7578289 | 7578208 | 7578208 | Missense_Mutation | T | C | p.H214R |
| JHC7_BONE | 7578177 | 7578289 | 7578211 | 7578211 | Missense_Mutation | C | A | p.R213L |
| HT55_LARGE_INTESTINE | 7578177 | 7578289 | 7578211 | 7578211 | Missense_Mutation | C | A | p.R213L |
| AN3CA_ENDOMETRIUM | 7578177 | 7578289 | 7578211 | 7578211 | Missense_Mutation | C | T | p.R213Q |
| MHHPREB1_HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 7578177 | 7578289 | 7578211 | 7578211 | Missense_Mutation | C | T | p.R213Q |
| RAJI_HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 7578177 | 7578289 | 7578211 | 7578211 | Missense_Mutation | C | T | p.R213Q |
| U118MG_CENTRAL_NERVOUS_SYSTEM | 7578177 | 7578289 | 7578211 | 7578211 | Missense_Mutation | C | T | p.R213Q |
| U138MG_CENTRAL_NERVOUS_SYSTEM | 7578177 | 7578289 | 7578211 | 7578211 | Missense_Mutation | C | T | p.R213Q |
| 42MGBA_CENTRAL_NERVOUS_SYSTEM | 7578177 | 7578289 | 7578217 | 7578217 | Missense_Mutation | G | A | p.T211I |
| CI1_HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 7578177 | 7578289 | 7578218 | 7578218 | Missense_Mutation | T | C | p.T211A |
| RH30_SOFT_TISSUE | 7578177 | 7578289 | 7578235 | 7578235 | Missense_Mutation | T | C | p.Y205C |
| SNU16_STOMACH | 7578177 | 7578289 | 7578235 | 7578235 | Missense_Mutation | T | A | p.Y205F |
| SJRH30_SOFT_TISSUE | 7578177 | 7578289 | 7578235 | 7578235 | Missense_Mutation | T | C | p.Y205C |
| NCIH1155_LUNG | 7578177 | 7578289 | 7578235 | 7578235 | Missense_Mutation | T | A | p.Y205F |
| HCC4006_LUNG | 7578177 | 7578289 | 7578236 | 7578236 | Missense_Mutation | A | G | p.Y205H |
| SW1353_BONE | 7578177 | 7578289 | 7578242 | 7578242 | Missense_Mutation | C | A | p.V203L |
| LN382_CENTRAL_NERVOUS_SYSTEM | 7578177 | 7578289 | 7578260 | 7578260 | Missense_Mutation | C | G | p.V197L |
| HCC56_LARGE_INTESTINE | 7578177 | 7578289 | 7578262 | 7578262 | Missense_Mutation | C | G | p.R196P |
| SNU1077_ENDOMETRIUM | 7578177 | 7578289 | 7578265 | 7578265 | Missense_Mutation | A | C | p.I195S |
| KYSE180_OESOPHAGUS | 7578177 | 7578289 | 7578265 | 7578265 | Missense_Mutation | A | G | p.I195T |
| COV318_OVARY | 7578177 | 7578289 | 7578266 | 7578266 | Missense_Mutation | T | A | p.I195F |
| MERO82_LUNG | 7578177 | 7578289 | 7578268 | 7578268 | Missense_Mutation | A | C | p.L194R |
| GSS_STOMACH | 7578177 | 7578289 | 7578268 | 7578268 | Missense_Mutation | A | C | p.L194R |
| HCC515_LUNG | 7578177 | 7578289 | 7578269 | 7578269 | Missense_Mutation | G | A | p.L194F |
| T47D_BREAST | 7578177 | 7578289 | 7578269 | 7578269 | Missense_Mutation | G | A | p.L194F |
| KYSE140_OESOPHAGUS | 7578177 | 7578289 | 7578271 | 7578271 | Missense_Mutation | T | C | p.H193R |
| HUG1N_STOMACH | 7578177 | 7578289 | 7578271 | 7578271 | Missense_Mutation | T | G | p.H193P |
| CAL27_UPPER_AERODIGESTIVE_TRACT | 7578177 | 7578289 | 7578271 | 7578271 | Missense_Mutation | T | A | p.H193L |
| EFM19_BREAST | 7578177 | 7578289 | 7578271 | 7578271 | Missense_Mutation | T | C | p.H193R |
| SKLU1_LUNG | 7578177 | 7578289 | 7578271 | 7578271 | Missense_Mutation | T | C | p.H193R |
| CHL1_SKIN | 7578177 | 7578289 | 7578271 | 7578271 | Missense_Mutation | T | C | p.H193R |
| HN_UPPER_AERODIGESTIVE_TRACT | 7578177 | 7578289 | 7578271 | 7578271 | Missense_Mutation | T | A | p.H193L |
| HMCB_SKIN | 7578177 | 7578289 | 7578271 | 7578271 | Missense_Mutation | T | C | p.H193R |
| SW13_ADRENAL_CORTEX | 7578177 | 7578289 | 7578272 | 7578272 | Missense_Mutation | G | A | p.H193Y |
| KNS60_CENTRAL_NERVOUS_SYSTEM | 7578177 | 7578289 | 7578272 | 7578272 | Missense_Mutation | G | A | p.H193Y |
| SNU1033_LARGE_INTESTINE | 7578177 | 7578289 | 7578280 | 7578280 | Missense_Mutation | G | A | p.P190L |
| EFO21_OVARY | 7579312 | 7579590 | 7579317 | 7579317 | Missense_Mutation | A | G | p.C124R |
| KYSE70_OESOPHAGUS | 7579312 | 7579590 | 7579327 | 7579327 | Missense_Mutation | C | A | p.K120N |
| LN464_CENTRAL_NERVOUS_SYSTEM | 7579312 | 7579590 | 7579349 | 7579349 | Missense_Mutation | A | G | p.F113S |
| PACADD165_PANCREAS | 7579312 | 7579590 | 7579349 | 7579349 | Missense_Mutation | A | G | p.F113S |
| SMZ1_HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 7579312 | 7579590 | 7579349 | 7579349 | Missense_Mutation | A | G | p.F113S |
| ACN_AUTONOMIC_GANGLIA | 7579312 | 7579590 | 7579349 | 7579349 | Missense_Mutation | A | G | p.F113S |
| SKMG1_CENTRAL_NERVOUS_SYSTEM | 7579312 | 7579590 | 7579349 | 7579349 | Missense_Mutation | A | C | p.F113C |
| UMUC3_URINARY_TRACT | 7579312 | 7579590 | 7579349 | 7579349 | Missense_Mutation | A | C | p.F113C |
| NBTU110_AUTONOMIC_GANGLIA | 7579312 | 7579590 | 7579350 | 7579350 | Missense_Mutation | A | G | p.F113L |
| YH13_CENTRAL_NERVOUS_SYSTEM | 7579312 | 7579590 | 7579350 | 7579350 | Missense_Mutation | A | C | p.F113V |
| JHUEM7_ENDOMETRIUM | 7579312 | 7579590 | 7579350 | 7579350 | Missense_Mutation | A | C | p.F113V |
| HS870T_FIBROBLAST | 7579312 | 7579590 | 7579358 | 7579358 | Missense_Mutation | C | G | p.R110P |
| HUH1_LIVER | 7579312 | 7579590 | 7579358 | 7579358 | Missense_Mutation | C | A | p.R110L |
| KYSE30_OESOPHAGUS | 7579312 | 7579590 | 7579358 | 7579358 | Missense_Mutation | C | A | p.R110L |
| TE11_OESOPHAGUS | 7579312 | 7579590 | 7579358 | 7579358 | Missense_Mutation | C | A | p.R110L |
| SCABER_URINARY_TRACT | 7579312 | 7579590 | 7579358 | 7579358 | Missense_Mutation | C | A | p.R110L |
| MOGGUVW_CENTRAL_NERVOUS_SYSTEM | 7579312 | 7579590 | 7579358 | 7579358 | Missense_Mutation | C | G | p.R110P |
| SAT_UPPER_AERODIGESTIVE_TRACT | 7579312 | 7579590 | 7579358 | 7579358 | Missense_Mutation | C | A | p.R110L |
| SKNDZ_AUTONOMIC_GANGLIA | 7579312 | 7579590 | 7579358 | 7579358 | Missense_Mutation | C | A | p.R110L |
| MKN45_STOMACH | 7579312 | 7579590 | 7579359 | 7579359 | Missense_Mutation | G | A | p.R110C |
| SKN3_UPPER_AERODIGESTIVE_TRACT | 7579312 | 7579590 | 7579369 | 7579369 | Missense_Mutation | G | C | p.S106R |
| KMS28BM_HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 7579312 | 7579590 | 7579374 | 7579374 | Missense_Mutation | C | G | p.G105R |
| LN229_CENTRAL_NERVOUS_SYSTEM | 7579312 | 7579590 | 7579394 | 7579394 | Missense_Mutation | G | A | p.P98L |
| HEC59_ENDOMETRIUM | 7579312 | 7579590 | 7579403 | 7579403 | Missense_Mutation | G | A | p.S95F |
| MFE319_ENDOMETRIUM | 7579312 | 7579590 | 7579467 | 7579467 | Missense_Mutation | C | A | p.A74S |
| CMK_HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 7579312 | 7579590 | 7579542 | 7579542 | Missense_Mutation | C | G | p.D49H |
| ISHIKAWAHERAKLIO02ER_ENDOMETRIUM | 7579312 | 7579590 | 7579542 | 7579542 | Missense_Mutation | C | G | p.D49H |
| SNU1040_LARGE_INTESTINE | 7579312 | 7579590 | 7579545 | 7579545 | Missense_Mutation | C | T | p.D48N |
| NCIH1623_LUNG | 7579312 | 7579590 | 7579580 | 7579580 | Missense_Mutation | G | A | p.P36L |
| NCIH1623_LUNG | 7579312 | 7579590 | 7579580 | 7579581 | Missense_Mutation | GG | AA | p.P36L |
| NCIH1623_LUNG | 7579312 | 7579590 | 7579581 | 7579581 | Missense_Mutation | G | A | p.P36S |
| COLO783_SKIN | 7579700 | 7579721 | 7579716 | 7579716 | Missense_Mutation | G | A | p.P27L |
| TCCSUP_URINARY_TRACT | 7573927 | 7574033 | 7573982 | 7573982 | Nonsense_Mutation | C | A | p.E349* |
| KYSE510_OESOPHAGUS | 7573927 | 7574033 | 7574000 | 7574000 | Nonsense_Mutation | C | A | p.E343* |
| C84_LARGE_INTESTINE | 7573927 | 7574033 | 7574003 | 7574003 | Nonsense_Mutation | G | A | p.R342* |
| CHLA32_BONE | 7573927 | 7574033 | 7574003 | 7574003 | Nonsense_Mutation | G | A | p.R342* |
| OVSAHO_OVARY | 7573927 | 7574033 | 7574003 | 7574003 | Nonsense_Mutation | G | A | p.R342* |
| TEN_ENDOMETRIUM | 7573927 | 7574033 | 7574003 | 7574003 | Nonsense_Mutation | G | A | p.R342* |
| UACC893_BREAST | 7573927 | 7574033 | 7574003 | 7574003 | Nonsense_Mutation | G | A | p.R342* |
| KNS42_CENTRAL_NERVOUS_SYSTEM | 7573927 | 7574033 | 7574003 | 7574003 | Nonsense_Mutation | G | A | p.R342* |
| NCIH630_LARGE_INTESTINE | 7573927 | 7574033 | 7574003 | 7574003 | Nonsense_Mutation | G | A | p.R342* |
| TE15_OESOPHAGUS | 7573927 | 7574033 | 7574003 | 7574003 | Nonsense_Mutation | G | A | p.R342* |
| NCIH1373_LUNG | 7573927 | 7574033 | 7574012 | 7574012 | Nonsense_Mutation | C | A | p.E339* |
| KYSE450_OESOPHAGUS | 7573927 | 7574033 | 7574012 | 7574012 | Nonsense_Mutation | C | A | p.E339* |
| 647V_URINARY_TRACT | 7573927 | 7574033 | 7574021 | 7574021 | Nonsense_Mutation | C | A | p.E336* |
| SAS_UPPER_AERODIGESTIVE_TRACT | 7573927 | 7574033 | 7574021 | 7574021 | Nonsense_Mutation | C | A | p.E336* |
| SN12C_KIDNEY | 7573927 | 7574033 | 7574021 | 7574021 | Nonsense_Mutation | C | A | p.E336* |
| UBLC1_URINARY_TRACT | 7576853 | 7576926 | 7576855 | 7576855 | Nonsense_Mutation | G | A | p.Q331* |
| NCIH2228_LUNG | 7576853 | 7576926 | 7576855 | 7576855 | Nonsense_Mutation | G | A | p.Q331* |
| INA6_HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 7576853 | 7576926 | 7576855 | 7576855 | Nonsense_Mutation | G | A | p.Q331* |
| NK92MI_HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 7576853 | 7576926 | 7576870 | 7576870 | Nonsense_Mutation | C | A | p.E326* |
| S117_SOFT_TISSUE | 7576853 | 7576926 | 7576870 | 7576870 | Nonsense_Mutation | C | A | p.E326* |
| HS746T_STOMACH | 7576853 | 7576926 | 7576891 | 7576891 | Nonsense_Mutation | T | A | p.K319* |
| LAMA84_HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 7576853 | 7576926 | 7576891 | 7576891 | Nonsense_Mutation | T | A | p.K319* |
| KARPAS422_HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 7576853 | 7576926 | 7576891 | 7576891 | Nonsense_Mutation | T | A | p.K319* |
| OCILY10_HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 7576853 | 7576926 | 7576891 | 7576891 | Nonsense_Mutation | T | A | p.K319* |
| REC1_HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 7576853 | 7576926 | 7576897 | 7576897 | Nonsense_Mutation | G | A | p.Q317* |
| GCT_SOFT_TISSUE | 7576853 | 7576926 | 7576897 | 7576897 | Nonsense_Mutation | G | A | p.Q317* |
| MEWO_SKIN | 7576853 | 7576926 | 7576897 | 7576897 | Nonsense_Mutation | G | A | p.Q317* |
| GCT_SOFT_TISSUE | 7576853 | 7576926 | 7576897 | 7576898 | Nonsense_Mutation | GG | AA | p.Q317* |
| PACADD161_PANCREAS | 7577019 | 7577155 | 7577022 | 7577022 | Nonsense_Mutation | G | A | p.R306* |
| JURLMK1_HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 7577019 | 7577155 | 7577022 | 7577022 | Nonsense_Mutation | G | A | p.R306* |
| MFE296_ENDOMETRIUM | 7577019 | 7577155 | 7577022 | 7577022 | Nonsense_Mutation | G | A | p.R306* |
| HCC1937_BREAST | 7577019 | 7577155 | 7577022 | 7577022 | Nonsense_Mutation | G | A | p.R306* |
| NCIH2804_PLEURA | 7577019 | 7577155 | 7577022 | 7577022 | Nonsense_Mutation | G | A | p.R306* |
| MOLT4_HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 7577019 | 7577155 | 7577022 | 7577022 | Nonsense_Mutation | G | A | p.R306* |
| RCM1_LARGE_INTESTINE | 7577019 | 7577155 | 7577022 | 7577022 | Nonsense_Mutation | G | A | p.R306* |
| CORL47_LUNG | 7577019 | 7577155 | 7577022 | 7577022 | Nonsense_Mutation | G | A | p.R306* |
| NCIH1339_LUNG | 7577019 | 7577155 | 7577046 | 7577046 | Nonsense_Mutation | C | A | p.E298* |
| SKMES1_LUNG | 7577019 | 7577155 | 7577046 | 7577046 | Nonsense_Mutation | C | A | p.E298* |
| HCC1569_BREAST | 7577019 | 7577155 | 7577058 | 7577058 | Nonsense_Mutation | C | A | p.E294* |
| ISTSL2_LUNG | 7577019 | 7577155 | 7577058 | 7577058 | Nonsense_Mutation | C | A | p.E294* |
| NCIH810_LUNG | 7577019 | 7577155 | 7577058 | 7577058 | Nonsense_Mutation | C | A | p.E294* |
| NCIH810_LUNG | 7577019 | 7577155 | 7577058 | 7577059 | Nonsense_Mutation | CC | AG | p.E294* |
| RI1_HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 7577019 | 7577155 | 7577058 | 7577058 | Nonsense_Mutation | C | A | p.E294* |
| NCIH1915_LUNG | 7577019 | 7577155 | 7577067 | 7577067 | Nonsense_Mutation | T | A | p.K291* |
| NCIH2286_LUNG | 7577019 | 7577155 | 7577067 | 7577067 | Nonsense_Mutation | T | A | p.K291* |
| P3HR1_HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 7577019 | 7577155 | 7577079 | 7577079 | Nonsense_Mutation | C | A | p.E287* |
| SAT_UPPER_AERODIGESTIVE_TRACT | 7577019 | 7577155 | 7577127 | 7577127 | Nonsense_Mutation | C | A | p.E271* |
| BFTC909_KIDNEY | 7578177 | 7578289 | 7578179 | 7578179 | Nonsense_Mutation | C | A | p.E224* |
| RCCFG2_KIDNEY | 7578177 | 7578289 | 7578211 | 7578212 | Nonsense_Mutation | CG | TA | p.R213* |
| TC71_BONE | 7578177 | 7578289 | 7578212 | 7578212 | Nonsense_Mutation | G | A | p.R213* |
| ESS1_ENDOMETRIUM | 7578177 | 7578289 | 7578212 | 7578212 | Nonsense_Mutation | G | A | p.R213* |
| HEC251_ENDOMETRIUM | 7578177 | 7578289 | 7578212 | 7578212 | Nonsense_Mutation | G | A | p.R213* |
| TE14_OESOPHAGUS | 7578177 | 7578289 | 7578212 | 7578212 | Nonsense_Mutation | G | A | p.R213* |
| DMS114_LUNG | 7578177 | 7578289 | 7578212 | 7578212 | Nonsense_Mutation | G | A | p.R213* |
| RERFGC1B_STOMACH | 7578177 | 7578289 | 7578212 | 7578212 | Nonsense_Mutation | G | A | p.R213* |
| HDQP1_BREAST | 7578177 | 7578289 | 7578212 | 7578212 | Nonsense_Mutation | G | A | p.R213* |
| HT115_LARGE_INTESTINE | 7578177 | 7578289 | 7578212 | 7578212 | Nonsense_Mutation | G | A | p.R213* |
| EMCBAC1_LUNG | 7578177 | 7578289 | 7578212 | 7578212 | Nonsense_Mutation | G | A | p.R213* |
| H3118_UPPER_AERODIGESTIVE_TRACT | 7578177 | 7578289 | 7578212 | 7578212 | Nonsense_Mutation | G | A | p.R213* |
| HCC2998_LARGE_INTESTINE | 7578177 | 7578289 | 7578212 | 7578212 | Nonsense_Mutation | G | A | p.R213* |
| IPC298_SKIN | 7578177 | 7578289 | 7578212 | 7578212 | Nonsense_Mutation | G | A | p.R213* |
| NBSUSSR_AUTONOMIC_GANGLIA | 7578177 | 7578289 | 7578212 | 7578212 | Nonsense_Mutation | G | A | p.R213* |
| SNU81_LARGE_INTESTINE | 7578177 | 7578289 | 7578212 | 7578212 | Nonsense_Mutation | G | A | p.R213* |
| SW684_SOFT_TISSUE | 7578177 | 7578289 | 7578212 | 7578212 | Nonsense_Mutation | G | A | p.R213* |
| JHOM1_OVARY | 7578177 | 7578289 | 7578212 | 7578212 | Nonsense_Mutation | G | A | p.R213* |
| SUPT11_HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 7578177 | 7578289 | 7578212 | 7578212 | Nonsense_Mutation | G | A | p.R213* |
| MOLT13_HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 7578177 | 7578289 | 7578212 | 7578212 | Nonsense_Mutation | G | A | p.R213* |
| NCIH1793_LUNG | 7578177 | 7578289 | 7578224 | 7578224 | Nonsense_Mutation | T | A | p.R209* |
| NCIH2141_LUNG | 7578177 | 7578289 | 7578224 | 7578224 | Nonsense_Mutation | T | A | p.R209* |
| C2BBE1_LARGE_INTESTINE | 7578177 | 7578289 | 7578239 | 7578239 | Nonsense_Mutation | C | A | p.E204* |
| EKVX_LUNG | 7578177 | 7578289 | 7578239 | 7578239 | Nonsense_Mutation | C | A | p.E204* |
| EKVX_LUNG | 7578177 | 7578289 | 7578239 | 7578240 | Nonsense_Mutation | CC | AA | p.E204* |
| CACO2_LARGE_INTESTINE | 7578177 | 7578289 | 7578239 | 7578239 | Nonsense_Mutation | C | A | p.E204* |
| PLCPRF5_LIVER | 7578177 | 7578289 | 7578254 | 7578254 | Nonsense_Mutation | C | A | p.G199* |
| YD38_UPPER_AERODIGESTIVE_TRACT | 7578177 | 7578289 | 7578254 | 7578254 | Nonsense_Mutation | C | A | p.G199* |
| JURKAT_HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 7578177 | 7578289 | 7578263 | 7578263 | Nonsense_Mutation | G | A | p.R196* |
| CALU6_LUNG | 7578177 | 7578289 | 7578263 | 7578263 | Nonsense_Mutation | G | A | p.R196* |
| H9_HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 7578177 | 7578289 | 7578263 | 7578263 | Nonsense_Mutation | G | A | p.R196* |
| P31FUJ_HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 7578177 | 7578289 | 7578263 | 7578263 | Nonsense_Mutation | G | A | p.R196* |
| HUT78_HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 7578177 | 7578289 | 7578263 | 7578263 | Nonsense_Mutation | G | A | p.R196* |
| BICR6_UPPER_AERODIGESTIVE_TRACT | 7578177 | 7578289 | 7578275 | 7578275 | Nonsense_Mutation | G | A | p.Q192* |
| SNU738_CENTRAL_NERVOUS_SYSTEM | 7578177 | 7578289 | 7578275 | 7578275 | Nonsense_Mutation | G | A | p.Q192* |
| IALM_LUNG | 7578177 | 7578289 | 7578275 | 7578275 | Nonsense_Mutation | G | A | p.Q192* |
| NCIH1688_LUNG | 7578177 | 7578289 | 7578275 | 7578275 | Nonsense_Mutation | G | A | p.Q192* |
| OACP4C_OESOPHAGUS | 7578177 | 7578289 | 7578275 | 7578275 | Nonsense_Mutation | G | A | p.Q192* |
| HPBALL_HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 7579312 | 7579590 | 7579315 | 7579315 | Nonsense_Mutation | G | T | p.C124* |
| SBC1_LUNG | 7579312 | 7579590 | 7579329 | 7579329 | Nonsense_Mutation | T | A | p.K120* |
| EPLC272H_LUNG | 7579312 | 7579590 | 7579366 | 7579366 | Nonsense_Mutation | G | C | p.Y107* |
| GT3TKB_STOMACH | 7579312 | 7579590 | 7579377 | 7579377 | Nonsense_Mutation | G | A | p.Q104* |
| RERFLCAI_LUNG | 7579312 | 7579590 | 7579377 | 7579377 | Nonsense_Mutation | G | A | p.Q104* |
| KYSE50_OESOPHAGUS | 7579312 | 7579590 | 7579386 | 7579386 | Nonsense_Mutation | T | A | p.K101* |
| SKGT4_OESOPHAGUS | 7579312 | 7579590 | 7579389 | 7579389 | Nonsense_Mutation | G | A | p.Q100* |
| HCC44_LUNG | 7579312 | 7579590 | 7579406 | 7579406 | Nonsense_Mutation | G | C | p.S94* |
| TFK1_BILIARY_TRACT | 7579312 | 7579590 | 7579414 | 7579414 | Nonsense_Mutation | C | T | p.W91* |
| MOLT13_HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 7579312 | 7579590 | 7579414 | 7579414 | Nonsense_Mutation | C | T | p.W91* |
| KMS18_HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 7579312 | 7579590 | 7579414 | 7579414 | Nonsense_Mutation | C | T | p.W91* |
| NCIH838_LUNG | 7579312 | 7579590 | 7579503 | 7579503 | Nonsense_Mutation | C | A | p.E62* |
| NCIH2126_LUNG | 7579312 | 7579590 | 7579503 | 7579503 | Nonsense_Mutation | C | A | p.E62* |
| DMS53_LUNG | 7579312 | 7579590 | 7579521 | 7579521 | Nonsense_Mutation | C | A | p.E56* |
| MDAMB361_BREAST | 7579312 | 7579590 | 7579521 | 7579521 | Nonsense_Mutation | C | A | p.E56* |
| UMUC5_URINARY_TRACT | 7579312 | 7579590 | 7579529 | 7579529 | Nonsense_Mutation | C | T | p.W53* |
| C80_LARGE_INTESTINE | 7579312 | 7579590 | 7579533 | 7579533 | Nonsense_Mutation | G | A | p.Q52* |
| SW403_LARGE_INTESTINE | 7579312 | 7579590 | 7579536 | 7579536 | Nonsense_Mutation | C | A | p.E51* |
| BICR78_UPPER_AERODIGESTIVE_TRACT | 7579312 | 7579590 | 7579575 | 7579575 | Nonsense_Mutation | G | A | p.Q38* |
| DANG_PANCREAS | 7576853 | 7576926 | 7576837 | 7576874 | Splice_Site | TCCCAAGACTTAGTACCTGAAGGGTGAAATATTCTCCA | - | p.GEYFTLQV325fs |
| 22RV1_PROSTATE | 7576853 | 7576926 | 7576854 | 7576854 | Splice_Site | T | C | p.Q331R |
| CCLFPEDS0008T_SOFT_TISSUE | 7576853 | 7576926 | 7576910 | 7576936 | Splice_Site | GGTGTTGTTGGGCAGTGCTAGGAAAGA | - | p.VFPSTA307del |
| BICR22_UPPER_AERODIGESTIVE_TRACT | 7576853 | 7576926 | 7576926 | 7576926 | Splice_Site | G | A | p.A307V |
| BICR22_UPPER_AERODIGESTIVE_TRACT | 7576853 | 7576926 | 7576926 | 7576927 | Splice_Site | GC | AA | p.G307V |
| HCC1195_LUNG | 7577019 | 7577155 | 7577150 | 7577159 | Splice_Site | TTACCACTAC | - | p.*W262fs |
| NB7_AUTONOMIC_GANGLIA | 7577019 | 7577155 | 7577154 | 7577154 | Splice_Site | C | T | p.G262S |
| TC106_BONE | 7578177 | 7578289 | 7578177 | 7578177 | Splice_Site | C | A | p.E224D |
| NCIH716_LARGE_INTESTINE | 7578177 | 7578289 | 7578177 | 7578177 | Splice_Site | C | A | p.E224D |
| RERFLCKJ_LUNG | 7578177 | 7578289 | 7578177 | 7578177 | Splice_Site | C | A | p.E224D |
| SNU398_LIVER | 7578177 | 7578289 | 7578177 | 7578177 | Splice_Site | C | T | p.E224E |
| MCC26_SKIN | 7579312 | 7579590 | 7579311 | 7579312 | Splice_Site | CC | TT | p.D126N |
| NCIH835_LUNG | 7579312 | 7579590 | 7579311 | 7579312 | Splice_Site | CC | AT | p.D126Y |
| RHJT_SOFT_TISSUE | 7579312 | 7579590 | 7579312 | 7579312 | Splice_Site | C | A | p.T125T |
| JURKAT_HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 7579312 | 7579590 | 7579312 | 7579312 | Splice_Site | C | T | p.T125T |
| PEER_HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 7579312 | 7579590 | 7579312 | 7579312 | Splice_Site | C | T | p.T125T |
| SEM_HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 7579312 | 7579590 | 7579312 | 7579312 | Splice_Site | C | T | p.T125T |
| SNU899_UPPER_AERODIGESTIVE_TRACT | 7579312 | 7579590 | 7579312 | 7579312 | Splice_Site | C | A | p.T125T |
| NCIH82_LUNG | 7579312 | 7579590 | 7579312 | 7579312 | Splice_Site | C | A | p.T125T |
| BE13_HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 7579312 | 7579590 | 7579312 | 7579312 | Splice_Site | C | T | p.T125T |
| CAPAN2_PANCREAS | 7579312 | 7579590 | 7579312 | 7579312 | Splice_Site | C | A | p.T125T |
| CORL32_LUNG | 7579312 | 7579590 | 7579312 | 7579312 | Splice_Site | C | A | p.T125T |
| EN_ENDOMETRIUM | 7579312 | 7579590 | 7579312 | 7579312 | Splice_Site | C | A | p.T125T |
| EW3_BONE | 7579312 | 7579590 | 7579312 | 7579312 | Splice_Site | C | T | p.T125T |
| KE37_HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 7579312 | 7579590 | 7579312 | 7579312 | Splice_Site | C | T | p.T125T |
| LU65_LUNG | 7579312 | 7579590 | 7579312 | 7579312 | Splice_Site | C | A | p.T125T |
| NCIH128_LUNG | 7579312 | 7579590 | 7579312 | 7579312 | Splice_Site | C | A | p.T125T |
| NCIH2347_LUNG | 7579312 | 7579590 | 7579312 | 7579312 | Splice_Site | C | T | p.T125T |
| SNU626_CENTRAL_NERVOUS_SYSTEM | 7579312 | 7579590 | 7579313 | 7579313 | Splice_Site | G | A | p.T125M |
| KARPAS45_HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 7579312 | 7579590 | 7579313 | 7579313 | Splice_Site | G | A | p.T125M |
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Splicing Quantitative Trait Loci (sQTL) in the exon skipping event for TP53 |
| sQTL information located at the skipped exons. |
| Exon skip ID | Chromosome | Three exons | Skippped exon | ENST | Cancer type | SNP id | Location | DNA change (ref/var) | P-value |
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Splicing Quantitative Trait Methylation (sQTM) in the skipped exon for TP53 |
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Survival analysis of Splicing Quantitative Trait Methylation (sQTM) in the skipped exon for TP53 |
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RelatedDrugs for TP53 |
| Approved drugs targeting this gene. (DrugBank Version 5.1.0 2018-04-02) |
| Gene | UniProtAcc | DrugBank ID | Drug name | Drug activity | Drug type | Drug status |
| P04637 | DB01593 | Zinc | Cellular tumor antigen p53 | small molecule | approved|investigational | |
| P04637 | DB14487 | Zinc acetate | Cellular tumor antigen p53 | small molecule | approved|investigational | |
| P04637 | DB14533 | Zinc chloride | Cellular tumor antigen p53 | small molecule | approved|investigational | |
| P04637 | DB00945 | Acetylsalicylic acid | Cellular tumor antigen p53 | small molecule | approved|vet_approved |
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RelatedDiseases for TP53 |
| Diseases associated with this gene. (DisGeNet 4.0) |
| Gene | Disease ID | Disease name | # pubmeds | Source |
| TP53 | C1835398 | LI-FRAUMENI SYNDROME 1 | 19 | CTD_human;UNIPROT |
| TP53 | C0009404 | Colorectal Neoplasms | 8 | CTD_human |
| TP53 | C0033578 | Prostatic Neoplasms | 6 | CTD_human;HPO |
| TP53 | C2239176 | Liver carcinoma | 6 | CTD_human;HPO |
| TP53 | C0024121 | Lung Neoplasms | 5 | CTD_human |
| TP53 | C1458155 | Mammary Neoplasms | 5 | CTD_human |
| TP53 | C0005695 | Bladder Neoplasm | 4 | CTD_human |
| TP53 | C0007134 | Renal Cell Carcinoma | 4 | CTD_human;HPO |
| TP53 | C0001418 | Adenocarcinoma | 3 | CTD_human |
| TP53 | C0007117 | Basal cell carcinoma | 3 | CTD_human |
| TP53 | C0007131 | Non-Small Cell Lung Carcinoma | 3 | CTD_human |
| TP53 | C0009375 | Colonic Neoplasms | 3 | CTD_human;HPO |
| TP53 | C0017638 | Glioma | 3 | CTD_human |
| TP53 | C0025202 | melanoma | 3 | CTD_human |
| TP53 | C0206686 | Adrenocortical carcinoma | 3 | CTD_human;HPO;ORPHANET |
| TP53 | C0001969 | Alcoholic Intoxication | 2 | PSYGENET |
| TP53 | C0001973 | Alcoholic Intoxication, Chronic | 2 | PSYGENET |
| TP53 | C0007137 | Squamous cell carcinoma | 2 | CTD_human |
| TP53 | C0014859 | Esophageal Neoplasms | 2 | CTD_human |
| TP53 | C0016978 | gallbladder neoplasm | 2 | CTD_human |
| TP53 | C0023903 | Liver neoplasms | 2 | CTD_human |
| TP53 | C0036920 | Sezary Syndrome | 2 | CTD_human |
| TP53 | C0038356 | Stomach Neoplasms | 2 | CTD_human;HPO |
| TP53 | C0149925 | Small cell carcinoma of lung | 2 | CTD_human;ORPHANET |
| TP53 | C0311375 | Arsenic Poisoning | 2 | CTD_human |
| TP53 | C0001430 | Adenoma | 1 | CTD_human |
| TP53 | C0001624 | Adrenal Gland Neoplasms | 1 | CTD_human |
| TP53 | C0002736 | Amyotrophic Lateral Sclerosis | 1 | CTD_human |
| TP53 | C0004698 | Balkan Nephropathy | 1 | CTD_human |
| TP53 | C0007138 | Carcinoma, Transitional Cell | 1 | CTD_human |
| TP53 | C0007194 | Hypertrophic Cardiomyopathy | 1 | CTD_human |
| TP53 | C0007273 | Carotid Artery Diseases | 1 | CTD_human |
| TP53 | C0007621 | Neoplastic Cell Transformation | 1 | CTD_human |
| TP53 | C0007786 | Brain Ischemia | 1 | CTD_human |
| TP53 | C0010606 | Adenoid Cystic Carcinoma | 1 | CTD_human |
| TP53 | C0011303 | Demyelinating Diseases | 1 | CTD_human |
| TP53 | C0011853 | Diabetes Mellitus, Experimental | 1 | CTD_human |
| TP53 | C0013990 | Pathological accumulation of air in tissues | 1 | CTD_human |
| TP53 | C0018923 | Hemangiosarcoma | 1 | CTD_human |
| TP53 | C0020538 | Hypertensive disease | 1 | CTD_human |
| TP53 | C0021361 | Female infertility | 1 | CTD_human |
| TP53 | C0021364 | Male infertility | 1 | CTD_human |
| TP53 | C0022116 | Ischemia | 1 | CTD_human |
| TP53 | C0022593 | Keratosis | 1 | CTD_human |
| TP53 | C0022783 | Vulvar Lichen Sclerosus | 1 | CTD_human |
| TP53 | C0023434 | Chronic Lymphocytic Leukemia | 1 | CTD_human;ORPHANET |
| TP53 | C0023897 | Liver Diseases, Parasitic | 1 | CTD_human |
| TP53 | C0023904 | Liver Neoplasms, Experimental | 1 | CTD_human |
| TP53 | C0024117 | Chronic Obstructive Airway Disease | 1 | CTD_human |
| TP53 | C0024809 | Marijuana Abuse | 1 | PSYGENET |
| TP53 | C0026640 | Mouth Neoplasms | 1 | CTD_human |
| TP53 | C0027627 | Neoplasm Metastasis | 1 | CTD_human |
| TP53 | C0029463 | Osteosarcoma | 1 | CTD_human;HPO |
| TP53 | C0030849 | Penile Neoplasms | 1 | CTD_human |
| TP53 | C0032578 | Polyploidy | 1 | CTD_human |
| TP53 | C0033860 | Psoriasis | 1 | CTD_human |
| TP53 | C0036341 | Schizophrenia | 1 | CTD_human |
| TP53 | C0037286 | Skin Neoplasms | 1 | CTD_human;HPO |
| TP53 | C0040100 | Thymoma | 1 | CTD_human |
| TP53 | C0040136 | Thyroid Neoplasm | 1 | CTD_human |
| TP53 | C0042065 | Genitourinary Neoplasms | 1 | CTD_human |
| TP53 | C0042076 | Urologic Neoplasms | 1 | CTD_human |
| TP53 | C0079772 | T-Cell Lymphoma | 1 | CTD_human |
| TP53 | C0079773 | Lymphoma, T-Cell, Cutaneous | 1 | CTD_human |
| TP53 | C0085136 | Central Nervous System Neoplasms | 1 | CTD_human |
| TP53 | C0085390 | Li-Fraumeni Syndrome | 1 | CTD_human;ORPHANET |
| TP53 | C0206681 | Adenocarcinoma, Clear Cell | 1 | CTD_human |
| TP53 | C0206698 | Cholangiocarcinoma | 1 | CTD_human |
| TP53 | C0262584 | Carcinoma, Small Cell | 1 | CTD_human |
| TP53 | C0279626 | Squamous cell carcinoma of esophagus | 1 | CTD_human |
| TP53 | C0279628 | Adenocarcinoma Of Esophagus | 1 | CTD_human |
| TP53 | C0345967 | Malignant mesothelioma | 1 | CTD_human |
| TP53 | C0677886 | Epithelial ovarian cancer | 1 | CTD_human |
| TP53 | C1168401 | Squamous cell carcinoma of the head and neck | 1 | CTD_human |
| TP53 | C1261473 | Sarcoma | 1 | CTD_human;HPO |
| TP53 | C1860789 | Leukemia, Megakaryoblastic, of Down Syndrome | 1 | CTD_human |
| TP53 | C1961102 | Precursor Cell Lymphoblastic Leukemia Lymphoma | 1 | CTD_human |
| TP53 | C2609414 | Acute kidney injury | 1 | CTD_human |
| TP53 | C2931713 | Chromosome 17 deletion | 1 | CTD_human |
| TP53 | C2931822 | Nasopharyngeal carcinoma | 1 | CTD_human |
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