| Exon skip ID | chr | Exons involved in exon skipping | Skipped exon | ENSG | ENSTs |
| exon_skip_453142 | 6 | 76311939:76312292:76331247:76331341:76332466:76332574 | 76331247:76331341 | ENSG00000112701.13 | ENST00000493959.2 |
| exon_skip_453143 | 6 | 76311939:76312292:76331247:76331341:76333615:76333676 | 76331247:76331341 | ENSG00000112701.13 | ENST00000370014.3,ENST00000327284.8,ENST00000447266.2 |
| exon_skip_453148 | 6 | 76331247:76331341:76332466:76332574:76333615:76333676 | 76332466:76332574 | ENSG00000112701.13 | ENST00000493959.2 |
| exon_skip_453151 | 6 | 76333615:76333676:76343296:76343442:76344422:76344527 | 76343296:76343442 | ENSG00000112701.13 | ENST00000370010.2,ENST00000370014.3,ENST00000483859.2,ENST00000493959.2,ENST00000327284.8,ENST00000447266.2 |
| exon_skip_453154 | 6 | 76343419:76343442:76344422:76344527:76357446:76357517 | 76344422:76344527 | ENSG00000112701.13 | ENST00000370010.2,ENST00000327284.8 |
| exon_skip_453156 | 6 | 76344422:76344527:76344695:76344716:76357446:76357517 | 76344695:76344716 | ENSG00000112701.13 | ENST00000370014.3 |
| exon_skip_453157 | 6 | 76344422:76344527:76350399:76350420:76357446:76357517 | 76350399:76350420 | ENSG00000112701.13 | ENST00000424947.2,ENST00000447266.2 |
| exon_skip_453158 | 6 | 76344422:76344527:76350402:76350420:76357446:76357517 | 76350402:76350420 | ENSG00000112701.13 | ENST00000483859.2 |
| exon_skip_453159 | 6 | 76344422:76344527:76357446:76357517:76368977:76369123 | 76357446:76357517 | ENSG00000112701.13 | ENST00000370010.2,ENST00000327284.8 |
| exon_skip_453160 | 6 | 76368977:76369123:76372936:76373234:76376427:76376657 | 76372936:76373234 | ENSG00000112701.13 | ENST00000370010.2,ENST00000370014.3,ENST00000327284.8,ENST00000424947.2,ENST00000447266.2 |
| exon_skip_453162 | 6 | 76380268:76380436:76385150:76385184:76385575:76385770 | 76385150:76385184 | ENSG00000112701.13 | ENST00000370010.2,ENST00000541192.1,ENST00000370014.3,ENST00000503501.1,ENST00000327284.8,ENST00000424947.2,ENST00000447266.2 |
| exon_skip_453165 | 6 | 76388526:76388643:76405519:76405639:76407140:76407233 | 76405519:76405639 | ENSG00000112701.13 | ENST00000370010.2,ENST00000541192.1,ENST00000370014.3,ENST00000474906.1,ENST00000503501.1,ENST00000447266.2 |
| exon_skip_453169 | 6 | 76407140:76407233:76412360:76412788:76419242:76419346 | 76412360:76412788 | ENSG00000112701.13 | ENST00000370010.2,ENST00000370014.3,ENST00000447266.2 |
| exon_skip_453175 | 6 | 76419242:76419346:76421043:76421132:76423228:76423297 | 76421043:76421132 | ENSG00000112701.13 | ENST00000370010.2,ENST00000541192.1,ENST00000370014.3,ENST00000503501.1,ENST00000447266.2 |
| exon_skip_453179 | 6 | 76421043:76421132:76423228:76423297:76423390:76423541 | 76423228:76423297 | ENSG00000112701.13 | ENST00000370010.2,ENST00000541192.1,ENST00000370014.3,ENST00000503501.1,ENST00000447266.2 |
| exon_skip_453181 | 6 | 76423228:76423297:76423390:76423541:76425100:76425593 | 76423390:76423541 | ENSG00000112701.13 | ENST00000370010.2,ENST00000541192.1,ENST00000370014.3,ENST00000503501.1,ENST00000447266.2 |
| Exon skip ID | chr | Exons involved in exon skipping | Skipped exon | ENSG | ENSTs |
| exon_skip_453142 | 6 | 76311939:76312292:76331247:76331341:76332466:76332574 | 76331247:76331341 | ENSG00000112701.13 | ENST00000493959.2 |
| exon_skip_453143 | 6 | 76311939:76312292:76331247:76331341:76333615:76333676 | 76331247:76331341 | ENSG00000112701.13 | ENST00000370014.3,ENST00000327284.8,ENST00000447266.2 |
| exon_skip_453148 | 6 | 76331247:76331341:76332466:76332574:76333615:76333676 | 76332466:76332574 | ENSG00000112701.13 | ENST00000493959.2 |
| exon_skip_453151 | 6 | 76333615:76333676:76343296:76343442:76344422:76344527 | 76343296:76343442 | ENSG00000112701.13 | ENST00000370010.2,ENST00000370014.3,ENST00000327284.8,ENST00000447266.2,ENST00000493959.2,ENST00000483859.2 |
| exon_skip_453154 | 6 | 76343419:76343442:76344422:76344527:76357446:76357517 | 76344422:76344527 | ENSG00000112701.13 | ENST00000370010.2,ENST00000327284.8 |
| exon_skip_453157 | 6 | 76344422:76344527:76350399:76350420:76357446:76357517 | 76350399:76350420 | ENSG00000112701.13 | ENST00000447266.2,ENST00000424947.2 |
| exon_skip_453158 | 6 | 76344422:76344527:76350402:76350420:76357446:76357517 | 76350402:76350420 | ENSG00000112701.13 | ENST00000483859.2 |
| exon_skip_453159 | 6 | 76344422:76344527:76357446:76357517:76368977:76369123 | 76357446:76357517 | ENSG00000112701.13 | ENST00000370010.2,ENST00000327284.8 |
| exon_skip_453160 | 6 | 76368977:76369123:76372936:76373234:76376427:76376657 | 76372936:76373234 | ENSG00000112701.13 | ENST00000370010.2,ENST00000370014.3,ENST00000327284.8,ENST00000447266.2,ENST00000424947.2 |
| exon_skip_453162 | 6 | 76380268:76380436:76385150:76385184:76385575:76385770 | 76385150:76385184 | ENSG00000112701.13 | ENST00000370010.2,ENST00000370014.3,ENST00000327284.8,ENST00000447266.2,ENST00000424947.2,ENST00000503501.1,ENST00000541192.1 |
| exon_skip_453165 | 6 | 76388526:76388643:76405519:76405639:76407140:76407233 | 76405519:76405639 | ENSG00000112701.13 | ENST00000370010.2,ENST00000370014.3,ENST00000447266.2,ENST00000503501.1,ENST00000541192.1,ENST00000474906.1 |
| exon_skip_453169 | 6 | 76407140:76407233:76412360:76412788:76419242:76419346 | 76412360:76412788 | ENSG00000112701.13 | ENST00000370010.2,ENST00000370014.3,ENST00000447266.2 |
| exon_skip_453175 | 6 | 76419242:76419346:76421043:76421132:76423228:76423297 | 76421043:76421132 | ENSG00000112701.13 | ENST00000370010.2,ENST00000370014.3,ENST00000447266.2,ENST00000503501.1,ENST00000541192.1 |
| exon_skip_453179 | 6 | 76421043:76421132:76423228:76423297:76423390:76423541 | 76423228:76423297 | ENSG00000112701.13 | ENST00000370010.2,ENST00000370014.3,ENST00000447266.2,ENST00000503501.1,ENST00000541192.1 |
| exon_skip_453181 | 6 | 76423228:76423297:76423390:76423541:76425100:76425593 | 76423390:76423541 | ENSG00000112701.13 | ENST00000370010.2,ENST00000370014.3,ENST00000447266.2,ENST00000503501.1,ENST00000541192.1 |
| Depth of coverage in three exons | Mutation description |
 | Sample: TCGA-C8-A26Z-01 |
| Cancer type: BRCA |
| ESID: exon_skip_453169 |
| Skipped exon start: 76412361 |
| Skipped exon end: 76412788 |
| Mutation start: 76412369 |
| Mutation end: 76412369 |
| Mutation type: Nonsense_Mutation |
| Reference seq: G |
| Mutation seq: A |
| AAchange: p.W766* |
exon_skip_453169_BRCA_TCGA-C8-A26Z-01.png
 |
 | Sample: TCGA-RY-A843-01 |
| Cancer type: LGG |
| ESID: exon_skip_453169 |
| Skipped exon start: 76412361 |
| Skipped exon end: 76412788 |
| Mutation start: 76412532 |
| Mutation end: 76412533 |
| Mutation type: Frame_Shift_Ins |
| Reference seq: - |
| Mutation seq: A |
| AAchange: p.A821fs |
exon_skip_453169_LGG_TCGA-RY-A843-01.png
 |
 | Sample: TCGA-AP-A0LH-01 |
| Cancer type: UCEC |
| ESID: exon_skip_453156 |
| Skipped exon start: 76344696 |
| Skipped exon end: 76344716 |
| Mutation start: 76344716 |
| Mutation end: 76344717 |
| Mutation type: Frame_Shift_Ins |
| Reference seq: - |
| Mutation seq: G |
| AAchange: p.K161fs |
exon_skip_304690_UCEC_TCGA-AP-A0LH-01.png
 |
exon_skip_304691_UCEC_TCGA-AP-A0LH-01.png
 |
exon_skip_453156_UCEC_TCGA-AP-A0LH-01.png
 |
exon_skip_49506_UCEC_TCGA-AP-A0LH-01.png
 |
exon_skip_92984_UCEC_TCGA-AP-A0LH-01.png
 |
| Sample | Skipped exon start | Skipped exon end | Mutation start | Mutation end | Mutation type | Reference seq | Mutation seq | AAchange |
| HCC1500_BREAST | 76331248 | 76331341 | 76331290 | 76331291 | Frame_Shift_Del | AT | - | p.N33fs |
| 2313287_STOMACH | 76423391 | 76423541 | 76423533 | 76423533 | Frame_Shift_Del | T | - | p.F1042fs |
| NUGC3_STOMACH | 76412361 | 76412788 | 76412559 | 76412560 | Frame_Shift_Ins | - | A | p.K830fs |
| LN443_CENTRAL_NERVOUS_SYSTEM | 76423391 | 76423541 | 76423532 | 76423533 | Frame_Shift_Ins | - | T | p.F1041fs |
| MDAMB468_BREAST | 76423391 | 76423541 | 76423532 | 76423533 | Frame_Shift_Ins | - | T | p.F1041fs |
| NCIH196_LUNG | 76423391 | 76423541 | 76423532 | 76423533 | Frame_Shift_Ins | - | T | p.F1041fs |
| NCIH69_LUNG | 76423391 | 76423541 | 76423532 | 76423533 | Frame_Shift_Ins | - | T | p.F1041fs |
| PFEIFFER_HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 76423391 | 76423541 | 76423532 | 76423533 | Frame_Shift_Ins | - | T | p.F1041fs |
| SIGM5_HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 76423391 | 76423541 | 76423532 | 76423533 | Frame_Shift_Ins | - | T | p.F1041fs |
| SKNSH_AUTONOMIC_GANGLIA | 76423391 | 76423541 | 76423532 | 76423533 | Frame_Shift_Ins | - | T | p.F1041fs |
| SNB75_CENTRAL_NERVOUS_SYSTEM | 76423391 | 76423541 | 76423532 | 76423533 | Frame_Shift_Ins | - | T | p.F1041fs |
| SNU601_STOMACH | 76423391 | 76423541 | 76423532 | 76423533 | Frame_Shift_Ins | - | T | p.F1041fs |
| T84_LARGE_INTESTINE | 76423391 | 76423541 | 76423532 | 76423533 | Frame_Shift_Ins | - | T | p.F1041fs |
| KNS60_CENTRAL_NERVOUS_SYSTEM | 76343297 | 76343442 | 76343330 | 76343332 | In_Frame_Del | TCT | - | p.S81del |
| SARC9371_BONE | 76343297 | 76343442 | 76343304 | 76343304 | Missense_Mutation | G | A | p.R72H |
| IOMMLEE_CENTRAL_NERVOUS_SYSTEM | 76343297 | 76343442 | 76343313 | 76343313 | Missense_Mutation | A | G | p.E75G |
| HEC6_ENDOMETRIUM | 76344423 | 76344527 | 76344439 | 76344439 | Missense_Mutation | A | G | p.T124A |
| HS742T_FIBROBLAST | 76344423 | 76344527 | 76344446 | 76344446 | Missense_Mutation | T | C | p.L126S |
| UBLC1_URINARY_TRACT | 76344423 | 76344527 | 76344460 | 76344460 | Missense_Mutation | G | C | p.V131L |
| KASUMI2_HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 76357447 | 76357517 | 76357479 | 76357479 | Missense_Mutation | A | G | p.E171G |
| MOLM16_HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 76357447 | 76357517 | 76357505 | 76357505 | Missense_Mutation | C | T | p.L180F |
| RHJT_SOFT_TISSUE | 76372937 | 76373234 | 76373040 | 76373040 | Missense_Mutation | A | G | p.N267S |
| LB831BLC_URINARY_TRACT | 76372937 | 76373234 | 76373081 | 76373081 | Missense_Mutation | G | A | p.E281K |
| HCC2450_LUNG | 76372937 | 76373234 | 76373085 | 76373085 | Missense_Mutation | A | T | p.K282M |
| SNU349_KIDNEY | 76372937 | 76373234 | 76373097 | 76373097 | Missense_Mutation | A | G | p.D286G |
| CMK_HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 76372937 | 76373234 | 76373169 | 76373169 | Missense_Mutation | C | G | p.A310G |
| BICR18_UPPER_AERODIGESTIVE_TRACT | 76405520 | 76405639 | 76405621 | 76405621 | Missense_Mutation | A | C | p.H726P |
| DAUDI_HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 76405520 | 76405639 | 76405621 | 76405621 | Missense_Mutation | A | C | p.H726P |
| BICR18_UPPER_AERODIGESTIVE_TRACT | 76405520 | 76405639 | 76405625 | 76405625 | Missense_Mutation | A | C | p.E727D |
| DAUDI_HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 76405520 | 76405639 | 76405625 | 76405625 | Missense_Mutation | A | C | p.E727D |
| HEC50B_ENDOMETRIUM | 76412361 | 76412788 | 76412389 | 76412389 | Missense_Mutation | T | G | p.F773V |
| MZ7MEL_SKIN | 76412361 | 76412788 | 76412419 | 76412419 | Missense_Mutation | C | T | p.P783S |
| SNU1040_LARGE_INTESTINE | 76412361 | 76412788 | 76412444 | 76412444 | Missense_Mutation | C | T | p.A791V |
| DERL2_HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 76412361 | 76412788 | 76412447 | 76412447 | Missense_Mutation | T | G | p.V792G |
| OCILY132_HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 76412361 | 76412788 | 76412447 | 76412447 | Missense_Mutation | T | G | p.V792G |
| SQ1_LUNG | 76412361 | 76412788 | 76412780 | 76412780 | Missense_Mutation | A | T | p.H903L |
| TE9_OESOPHAGUS | 76421044 | 76421132 | 76421074 | 76421074 | Missense_Mutation | G | A | p.D951N |
| BICR18_UPPER_AERODIGESTIVE_TRACT | 76421044 | 76421132 | 76421122 | 76421122 | Missense_Mutation | A | G | p.I967V |
| CHL1_SKIN | 76423391 | 76423541 | 76423432 | 76423432 | Missense_Mutation | G | A | p.R1007K |
| HMCB_SKIN | 76423391 | 76423541 | 76423432 | 76423432 | Missense_Mutation | G | A | p.R1007K |
| IGROV1_OVARY | 76423391 | 76423541 | 76423501 | 76423501 | Missense_Mutation | G | A | p.C1030Y |
| EFM192A_BREAST | 76331248 | 76331341 | 76331310 | 76331310 | Nonsense_Mutation | G | T | p.E39* |
| Exon skip ID | Chromosome | Three exons | Skippped exon | ENST | Cancer type | SNP id | Location | DNA change (ref/var) | P-value |
| exon_skip_453154 | 6 | 76343419:76343442:76344422:76344527:76357446:76357517 | 76344422:76344527 | ENST00000370010.2,ENST00000327284.8 | COAD | rs17414086 | chr6:76344431 | C/T | 2.59e-05
|
| exon_skip_453154 | 6 | 76343419:76343442:76344422:76344527:76357446:76357517 | 76344422:76344527 | ENST00000370010.2,ENST00000327284.8 | COAD | rs17414086 | chr6:76344431 | C/T | 2.59e-05
|
| exon_skip_453154 | 6 | 76343419:76343442:76344422:76344527:76357446:76357517 | 76344422:76344527 | ENST00000370010.2,ENST00000327284.8 | BLCA | rs17414086 | chr6:76344431 | C/T | 1.26e-03
|
| exon_skip_453154 | 6 | 76343419:76343442:76344422:76344527:76357446:76357517 | 76344422:76344527 | ENST00000370010.2,ENST00000327284.8 | BLCA | rs17414086 | chr6:76344431 | C/T | 1.26e-03
|
| exon_skip_453154 | 6 | 76343419:76343442:76344422:76344527:76357446:76357517 | 76344422:76344527 | ENST00000370010.2,ENST00000327284.8 | HNSC | rs17414086 | chr6:76344431 | C/T | 3.89e-04
|
| exon_skip_453154 | 6 | 76343419:76343442:76344422:76344527:76357446:76357517 | 76344422:76344527 | ENST00000370010.2,ENST00000327284.8 | HNSC | rs17414086 | chr6:76344431 | C/T | 3.89e-04
|
| exon_skip_453154 | 6 | 76343419:76343442:76344422:76344527:76357446:76357517 | 76344422:76344527 | ENST00000370010.2,ENST00000327284.8 | KIRP | rs17414086 | chr6:76344431 | C/T | 4.20e-06
|
| exon_skip_453154 | 6 | 76343419:76343442:76344422:76344527:76357446:76357517 | 76344422:76344527 | ENST00000370010.2,ENST00000327284.8 | KIRP | rs17414086 | chr6:76344431 | C/T | 4.20e-06
|
| exon_skip_453154 | 6 | 76343419:76343442:76344422:76344527:76357446:76357517 | 76344422:76344527 | ENST00000370010.2,ENST00000327284.8 | LGG | rs17414086 | chr6:76344431 | C/T | 1.82e-03
|
| exon_skip_453154 | 6 | 76343419:76343442:76344422:76344527:76357446:76357517 | 76344422:76344527 | ENST00000370010.2,ENST00000327284.8 | LGG | rs17414086 | chr6:76344431 | C/T | 1.82e-03
|
| exon_skip_453154 | 6 | 76343419:76343442:76344422:76344527:76357446:76357517 | 76344422:76344527 | ENST00000370010.2,ENST00000327284.8 | KIRC | rs17414086 | chr6:76344431 | C/T | 4.65e-05
|
| exon_skip_453154 | 6 | 76343419:76343442:76344422:76344527:76357446:76357517 | 76344422:76344527 | ENST00000370010.2,ENST00000327284.8 | KIRC | rs17414086 | chr6:76344431 | C/T | 4.66e-05
|
| exon_skip_453154 | 6 | 76343419:76343442:76344422:76344527:76357446:76357517 | 76344422:76344527 | ENST00000370010.2,ENST00000327284.8 | LUAD | rs17414086 | chr6:76344431 | C/T | 1.89e-03
|
| exon_skip_453154 | 6 | 76343419:76343442:76344422:76344527:76357446:76357517 | 76344422:76344527 | ENST00000370010.2,ENST00000327284.8 | LUAD | rs17414086 | chr6:76344431 | C/T | 1.89e-03
|
| exon_skip_453154 | 6 | 76343419:76343442:76344422:76344527:76357446:76357517 | 76344422:76344527 | ENST00000370010.2,ENST00000327284.8 | LUSC | rs17414086 | chr6:76344431 | C/T | 3.15e-03
|
| exon_skip_453154 | 6 | 76343419:76343442:76344422:76344527:76357446:76357517 | 76344422:76344527 | ENST00000370010.2,ENST00000327284.8 | LUSC | rs17414086 | chr6:76344431 | C/T | 3.15e-03
|
| exon_skip_453154 | 6 | 76343419:76343442:76344422:76344527:76357446:76357517 | 76344422:76344527 | ENST00000370010.2,ENST00000327284.8 | PRAD | rs17414086 | chr6:76344431 | C/T | 1.58e-03
|
| exon_skip_453154 | 6 | 76343419:76343442:76344422:76344527:76357446:76357517 | 76344422:76344527 | ENST00000370010.2,ENST00000327284.8 | PRAD | rs17414086 | chr6:76344431 | C/T | 1.58e-03
|
| exon_skip_453154 | 6 | 76343419:76343442:76344422:76344527:76357446:76357517 | 76344422:76344527 | ENST00000370010.2,ENST00000327284.8 | TGCT | rs17414086 | chr6:76344431 | C/T | 2.60e-07
|
| exon_skip_453154 | 6 | 76343419:76343442:76344422:76344527:76357446:76357517 | 76344422:76344527 | ENST00000370010.2,ENST00000327284.8 | TGCT | rs17414086 | chr6:76344431 | C/T | 2.61e-07
|
| exon_skip_453154 | 6 | 76343419:76343442:76344422:76344527:76357446:76357517 | 76344422:76344527 | ENST00000370010.2,ENST00000327284.8 | THCA | rs17414086 | chr6:76344431 | C/T | 1.12e-04
|
| exon_skip_453154 | 6 | 76343419:76343442:76344422:76344527:76357446:76357517 | 76344422:76344527 | ENST00000370010.2,ENST00000327284.8 | THCA | rs17414086 | chr6:76344431 | C/T | 1.12e-04
|