Exon skip ID | chr | Exons involved in exon skipping | Skipped exon | ENSG | ENSTs |
exon_skip_114672 | 14 | 75601490:75601709:75602365:75602589:75614366:75614440 | 75602365:75602589 | ENSG00000170348.4 | ENST00000555036.1 |
exon_skip_114673 | 14 | 75601490:75601709:75602462:75602589:75614366:75614440 | 75602462:75602589 | ENSG00000170348.4 | ENST00000556969.1,ENST00000557670.1,ENST00000303575.4 |
exon_skip_114674 | 14 | 75602462:75602589:75605776:75605874:75614366:75614440 | 75605776:75605874 | ENSG00000170348.4 | ENST00000555873.1 |
exon_skip_114675 | 14 | 75602462:75602589:75614366:75614440:75618734:75618846 | 75614366:75614440 | ENSG00000170348.4 | ENST00000303575.4 |
exon_skip_114681 | 14 | 75614366:75614440:75618734:75618846:75643057:75643300 | 75618734:75618846 | ENSG00000170348.4 | ENST00000555873.1,ENST00000555085.1 |
Exon skip ID | chr | Exons involved in exon skipping | Skipped exon | ENSG | ENSTs |
exon_skip_114672 | 14 | 75601490:75601709:75602365:75602589:75614366:75614440 | 75602365:75602589 | ENSG00000170348.4 | ENST00000555036.1 |
exon_skip_114673 | 14 | 75601490:75601709:75602462:75602589:75614366:75614440 | 75602462:75602589 | ENSG00000170348.4 | ENST00000303575.4,ENST00000556969.1,ENST00000557670.1 |
exon_skip_114674 | 14 | 75602462:75602589:75605776:75605874:75614366:75614440 | 75605776:75605874 | ENSG00000170348.4 | ENST00000555873.1 |
exon_skip_114675 | 14 | 75602462:75602589:75614366:75614440:75618734:75618846 | 75614366:75614440 | ENSG00000170348.4 | ENST00000303575.4 |
exon_skip_114681 | 14 | 75614366:75614440:75618734:75618846:75643057:75643300 | 75618734:75618846 | ENSG00000170348.4 | ENST00000555873.1,ENST00000555085.1 |
Depth of coverage in three exons | Mutation description |
| Sample: TCGA-AX-A0J0-01 |
Cancer type: UCEC |
ESID: exon_skip_114672 |
Skipped exon start: 75602366 |
Skipped exon end: 75602589 |
Mutation start: 75602547 |
Mutation end: 75602547 |
Mutation type: Nonsense_Mutation |
Reference seq: G |
Mutation seq: A |
AAchange: p.R152* |
| Sample: TCGA-AX-A0J0-01 |
Cancer type: UCEC |
ESID: exon_skip_114673 |
Skipped exon start: 75602463 |
Skipped exon end: 75602589 |
Mutation start: 75602547 |
Mutation end: 75602547 |
Mutation type: Nonsense_Mutation |
Reference seq: G |
Mutation seq: A |
AAchange: p.R152* |
exon_skip_114672_UCEC_TCGA-AX-A0J0-01.png
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exon_skip_145114_UCEC_TCGA-AX-A0J0-01.png
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exon_skip_148176_UCEC_TCGA-AX-A0J0-01.png
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exon_skip_148178_UCEC_TCGA-AX-A0J0-01.png
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exon_skip_26303_UCEC_TCGA-AX-A0J0-01.png
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exon_skip_316320_UCEC_TCGA-AX-A0J0-01.png
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exon_skip_366628_UCEC_TCGA-AX-A0J0-01.png
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exon_skip_422781_UCEC_TCGA-AX-A0J0-01.png
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exon_skip_440271_UCEC_TCGA-AX-A0J0-01.png
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exon_skip_47562_UCEC_TCGA-AX-A0J0-01.png
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exon_skip_500520_UCEC_TCGA-AX-A0J0-01.png
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exon_skip_60290_UCEC_TCGA-AX-A0J0-01.png
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exon_skip_60294_UCEC_TCGA-AX-A0J0-01.png
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Exon skip ID | Chromosome | Three exons | Skippped exon | ENST | Cancer type | SNP id | Location | DNA change (ref/var) | P-value |
exon_skip_114674 | 14 | 75602462:75602589:75605776:75605874:75614366:75614440 | 75605776:75605874 | ENST00000555873.1 | ACC | rs1047418 | chr14:75605792 | A/G | 7.66e-05
|
exon_skip_114674 | 14 | 75602462:75602589:75605776:75605874:75614366:75614440 | 75605776:75605874 | ENST00000555873.1 | GBM | rs1047418 | chr14:75605792 | A/G | 2.80e-23
|
exon_skip_114674 | 14 | 75602462:75602589:75605776:75605874:75614366:75614440 | 75605776:75605874 | ENST00000555873.1 | CESC | rs1047418 | chr14:75605792 | A/G | 7.66e-14
|
exon_skip_114674 | 14 | 75602462:75602589:75605776:75605874:75614366:75614440 | 75605776:75605874 | ENST00000555873.1 | COAD | rs1047418 | chr14:75605792 | A/G | 4.72e-30
|
exon_skip_114674 | 14 | 75602462:75602589:75605776:75605874:75614366:75614440 | 75605776:75605874 | ENST00000555873.1 | BLCA | rs1047418 | chr14:75605792 | A/G | 6.78e-19
|
exon_skip_114674 | 14 | 75602462:75602589:75605776:75605874:75614366:75614440 | 75605776:75605874 | ENST00000555873.1 | ESCA | rs1047418 | chr14:75605792 | A/G | 2.45e-14
|
exon_skip_114674 | 14 | 75602462:75602589:75605776:75605874:75614366:75614440 | 75605776:75605874 | ENST00000555873.1 | HNSC | rs1047418 | chr14:75605792 | A/G | 2.24e-46
|
exon_skip_114674 | 14 | 75602462:75602589:75605776:75605874:75614366:75614440 | 75605776:75605874 | ENST00000555873.1 | LAML | rs1047418 | chr14:75605792 | A/G | 1.25e-04
|
exon_skip_114674 | 14 | 75602462:75602589:75605776:75605874:75614366:75614440 | 75605776:75605874 | ENST00000555873.1 | KIRP | rs1047418 | chr14:75605792 | A/G | 8.41e-14
|
exon_skip_114674 | 14 | 75602462:75602589:75605776:75605874:75614366:75614440 | 75605776:75605874 | ENST00000555873.1 | LGG | rs1047418 | chr14:75605792 | A/G | 3.41e-85
|
exon_skip_114674 | 14 | 75602462:75602589:75605776:75605874:75614366:75614440 | 75605776:75605874 | ENST00000555873.1 | KIRC | rs1047418 | chr14:75605792 | A/G | 2.26e-51
|
exon_skip_114674 | 14 | 75602462:75602589:75605776:75605874:75614366:75614440 | 75605776:75605874 | ENST00000555873.1 | LUAD | rs1047418 | chr14:75605792 | A/G | 5.64e-49
|
exon_skip_114674 | 14 | 75602462:75602589:75605776:75605874:75614366:75614440 | 75605776:75605874 | ENST00000555873.1 | MESO | rs1047418 | chr14:75605792 | A/G | 6.03e-07
|
exon_skip_114674 | 14 | 75602462:75602589:75605776:75605874:75614366:75614440 | 75605776:75605874 | ENST00000555873.1 | LUSC | rs1047418 | chr14:75605792 | A/G | 1.69e-64
|
exon_skip_114674 | 14 | 75602462:75602589:75605776:75605874:75614366:75614440 | 75605776:75605874 | ENST00000555873.1 | OV | rs1047418 | chr14:75605792 | A/G | 4.23e-32
|
exon_skip_114674 | 14 | 75602462:75602589:75605776:75605874:75614366:75614440 | 75605776:75605874 | ENST00000555873.1 | READ | rs1047418 | chr14:75605792 | A/G | 3.45e-12
|
exon_skip_114674 | 14 | 75602462:75602589:75605776:75605874:75614366:75614440 | 75605776:75605874 | ENST00000555873.1 | PCPG | rs1047418 | chr14:75605792 | A/G | 4.58e-27
|
exon_skip_114674 | 14 | 75602462:75602589:75605776:75605874:75614366:75614440 | 75605776:75605874 | ENST00000555873.1 | PAAD | rs1047418 | chr14:75605792 | A/G | 1.06e-12
|
exon_skip_114674 | 14 | 75602462:75602589:75605776:75605874:75614366:75614440 | 75605776:75605874 | ENST00000555873.1 | PRAD | rs1047418 | chr14:75605792 | A/G | 1.54e-72
|
exon_skip_114674 | 14 | 75602462:75602589:75605776:75605874:75614366:75614440 | 75605776:75605874 | ENST00000555873.1 | SARC | rs1047418 | chr14:75605792 | A/G | 1.70e-20
|
exon_skip_114674 | 14 | 75602462:75602589:75605776:75605874:75614366:75614440 | 75605776:75605874 | ENST00000555873.1 | THYM | rs1047418 | chr14:75605792 | A/G | 1.57e-05
|
exon_skip_114674 | 14 | 75602462:75602589:75605776:75605874:75614366:75614440 | 75605776:75605874 | ENST00000555873.1 | TGCT | rs1047418 | chr14:75605792 | A/G | 3.27e-17
|
exon_skip_114674 | 14 | 75602462:75602589:75605776:75605874:75614366:75614440 | 75605776:75605874 | ENST00000555873.1 | SKCM | rs1047418 | chr14:75605792 | A/G | 3.05e-11
|
exon_skip_114674 | 14 | 75602462:75602589:75605776:75605874:75614366:75614440 | 75605776:75605874 | ENST00000555873.1 | STAD | rs1047418 | chr14:75605792 | A/G | 1.81e-21
|
exon_skip_114674 | 14 | 75602462:75602589:75605776:75605874:75614366:75614440 | 75605776:75605874 | ENST00000555873.1 | THCA | rs1047418 | chr14:75605792 | A/G | 1.58e-66
|
exon_skip_114674 | 14 | 75602462:75602589:75605776:75605874:75614366:75614440 | 75605776:75605874 | ENST00000555873.1 | UVM | rs1047418 | chr14:75605792 | A/G | 3.90e-10
|
exon_skip_114674 | 14 | 75602462:75602589:75605776:75605874:75614366:75614440 | 75605776:75605874 | ENST00000555873.1 | UCEC | rs1047418 | chr14:75605792 | A/G | 3.32e-15
|