Exon skip ID | chr | Exons involved in exon skipping | Skipped exon | ENSG | ENSTs |
exon_skip_88530 | 12 | 131356640:131356671:131357128:131357162:131357380:131357457 | 131357128:131357162 | ENSG00000132341.7 | ENST00000535090.1 |
exon_skip_88532 | 12 | 131356640:131356671:131357128:131357174:131357380:131357457 | 131357128:131357174 | ENSG00000132341.7 | ENST00000392367.3 |
exon_skip_88537 | 12 | 131356640:131356671:131357128:131357465:131357547:131357673 | 131357128:131357465 | ENSG00000132341.7 | ENST00000477395.1 |
exon_skip_88539 | 12 | 131356640:131356671:131357380:131357457:131357547:131357673 | 131357380:131357457 | ENSG00000132341.7 | ENST00000541630.1 |
exon_skip_88540 | 12 | 131356640:131356671:131357380:131357465:131357547:131357673 | 131357380:131357465 | ENSG00000132341.7 | ENST00000448750.3,ENST00000536606.1,ENST00000254675.3 |
exon_skip_88547 | 12 | 131357128:131357174:131357380:131357465:131357547:131357673 | 131357380:131357465 | ENSG00000132341.7 | ENST00000543796.1,ENST00000392369.2,ENST00000392367.3 |
exon_skip_88551 | 12 | 131357547:131357673:131358578:131358629:131359090:131359278 | 131358578:131358629 | ENSG00000132341.7 | ENST00000392367.3 |
exon_skip_88552 | 12 | 131357547:131357673:131359090:131359278:131360156:131360184 | 131359090:131359278 | ENSG00000132341.7 | ENST00000541630.1,ENST00000543796.1,ENST00000477395.1,ENST00000392369.2,ENST00000448750.3,ENST00000535090.1,ENST00000254675.3 |
exon_skip_88553 | 12 | 131357547:131357673:131359095:131359278:131360156:131360184 | 131359095:131359278 | ENSG00000132341.7 | ENST00000536606.1 |
Exon skip ID | chr | Exons involved in exon skipping | Skipped exon | ENSG | ENSTs |
exon_skip_88530 | 12 | 131356640:131356671:131357128:131357162:131357380:131357457 | 131357128:131357162 | ENSG00000132341.7 | ENST00000535090.1 |
exon_skip_88532 | 12 | 131356640:131356671:131357128:131357174:131357380:131357457 | 131357128:131357174 | ENSG00000132341.7 | ENST00000392367.3 |
exon_skip_88537 | 12 | 131356640:131356671:131357128:131357465:131357547:131357673 | 131357128:131357465 | ENSG00000132341.7 | ENST00000477395.1 |
exon_skip_88539 | 12 | 131356640:131356671:131357380:131357457:131357547:131357673 | 131357380:131357457 | ENSG00000132341.7 | ENST00000541630.1 |
exon_skip_88540 | 12 | 131356640:131356671:131357380:131357465:131357547:131357673 | 131357380:131357465 | ENSG00000132341.7 | ENST00000448750.3,ENST00000536606.1,ENST00000254675.3 |
exon_skip_88547 | 12 | 131357128:131357174:131357380:131357465:131357547:131357673 | 131357380:131357465 | ENSG00000132341.7 | ENST00000543796.1,ENST00000392369.2,ENST00000392367.3 |
exon_skip_88551 | 12 | 131357547:131357673:131358578:131358629:131359090:131359278 | 131358578:131358629 | ENSG00000132341.7 | ENST00000392367.3 |
exon_skip_88552 | 12 | 131357547:131357673:131359090:131359278:131360156:131360184 | 131359090:131359278 | ENSG00000132341.7 | ENST00000543796.1,ENST00000448750.3,ENST00000541630.1,ENST00000477395.1,ENST00000392369.2,ENST00000254675.3,ENST00000535090.1 |
exon_skip_88553 | 12 | 131357547:131357673:131359095:131359278:131360156:131360184 | 131359095:131359278 | ENSG00000132341.7 | ENST00000536606.1 |
Cancer type | Sample | ESID | Skipped exon start | Skipped exon end | Mutation start | Mutation end | Mutation type | Reference seq | Mutation seq | AAchange |
HNSC | TCGA-CQ-5334-01 | exon_skip_88552 exon_skip_88553
| 131359091 | 131359278 | 131359130 | 131359133 | Frame_Shift_Del | TTAC | - | p.V96fs |
HNSC | TCGA-CQ-5334-01 | exon_skip_88552 exon_skip_88553
| 131359091 | 131359278 | 131359130 | 131359133 | Frame_Shift_Del | TTAC | - | p.VT96fs |
HNSC | TCGA-CQ-5334-01 | exon_skip_88552 exon_skip_88553
| 131359096 | 131359278 | 131359130 | 131359133 | Frame_Shift_Del | TTAC | - | p.V96fs |
HNSC | TCGA-CQ-5334-01 | exon_skip_88552 exon_skip_88553
| 131359096 | 131359278 | 131359130 | 131359133 | Frame_Shift_Del | TTAC | - | p.VT96fs |
BRCA | TCGA-D8-A140-01 | exon_skip_88552 exon_skip_88553
| 131359091 | 131359278 | 131359172 | 131359172 | Frame_Shift_Del | G | - | p.R110fs |
BRCA | TCGA-D8-A140-01 | exon_skip_88552 exon_skip_88553
| 131359096 | 131359278 | 131359172 | 131359172 | Frame_Shift_Del | G | - | p.R110fs |
COAD | TCGA-A6-6650-01 | exon_skip_88552 exon_skip_88553
| 131359091 | 131359278 | 131359261 | 131359261 | Nonsense_Mutation | C | T | p.R140X |
COAD | TCGA-A6-6650-01 | exon_skip_88552 exon_skip_88553
| 131359096 | 131359278 | 131359261 | 131359261 | Nonsense_Mutation | C | T | p.R140X |
SKCM | TCGA-EE-A3J4-06 | exon_skip_88539
| 131357381 | 131357457 | 131357380 | 131357380 | Splice_Site | G | T | . |
SKCM | TCGA-EE-A3J4-06 | exon_skip_88540 exon_skip_88547
| 131357381 | 131357465 | 131357380 | 131357380 | Splice_Site | G | T | . |
Depth of coverage in three exons | Mutation description |
| Sample: TCGA-A6-6650-01 |
Cancer type: COAD |
ESID: exon_skip_88553 |
Skipped exon start: 131359091 |
Skipped exon end: 131359278 |
Mutation start: 131359261 |
Mutation end: 131359261 |
Mutation type: Nonsense_Mutation |
Reference seq: C |
Mutation seq: T |
AAchange: p.R140X |
| Sample: TCGA-A6-6650-01 |
Cancer type: COAD |
ESID: exon_skip_88553 |
Skipped exon start: 131359096 |
Skipped exon end: 131359278 |
Mutation start: 131359261 |
Mutation end: 131359261 |
Mutation type: Nonsense_Mutation |
Reference seq: C |
Mutation seq: T |
AAchange: p.R140X |
exon_skip_62194_COAD_TCGA-A6-6650-01.png
|
exon_skip_88552_COAD_TCGA-A6-6650-01.png
|
| Sample: TCGA-EE-A3J4-06 |
Cancer type: SKCM |
ESID: exon_skip_88539 |
Skipped exon start: 131357381 |
Skipped exon end: 131357457 |
Mutation start: 131357380 |
Mutation end: 131357380 |
Mutation type: Splice_Site |
Reference seq: G |
Mutation seq: T |
AAchange: . |
| Sample: TCGA-EE-A3J4-06 |
Cancer type: SKCM |
ESID: exon_skip_88547 |
Skipped exon start: 131357381 |
Skipped exon end: 131357465 |
Mutation start: 131357380 |
Mutation end: 131357380 |
Mutation type: Splice_Site |
Reference seq: G |
Mutation seq: T |
AAchange: . |
exon_skip_346530_SKCM_TCGA-EE-A3J4-06.png
|
exon_skip_88547_SKCM_TCGA-EE-A3J4-06.png
|