| Exon skip ID | chr | Exons involved in exon skipping | Skipped exon | ENSG | ENSTs |
| exon_skip_32244 | 1 | 155165635:155165690:155165777:155165917:155166831:155167000 | 155165777:155165917 | ENSG00000169231.9 | ENST00000457183.2,ENST00000541576.1,ENST00000368378.3,ENST00000541990.1,ENST00000469769.1 |
| exon_skip_32245 | 1 | 155166831:155167004:155167253:155167450:155167670:155167719 | 155167253:155167450 | ENSG00000169231.9 | ENST00000457183.2,ENST00000541576.1,ENST00000368378.3,ENST00000541990.1 |
| exon_skip_32249 | 1 | 155169785:155169904:155170241:155170401:155170687:155170795 | 155170241:155170401 | ENSG00000169231.9 | ENST00000457183.2,ENST00000541576.1,ENST00000368378.3,ENST00000541990.1 |
| exon_skip_32250 | 1 | 155170246:155170401:155170687:155170795:155170884:155170995 | 155170687:155170795 | ENSG00000169231.9 | ENST00000486260.1,ENST00000457183.2,ENST00000368378.3,ENST00000541990.1 |
| exon_skip_32251 | 1 | 155170246:155170401:155170687:155170795:155171207:155171360 | 155170687:155170795 | ENSG00000169231.9 | ENST00000541576.1 |
| exon_skip_32255 | 1 | 155170689:155170795:155170884:155170995:155171207:155171360 | 155170884:155170995 | ENSG00000169231.9 | ENST00000486260.1,ENST00000457183.2,ENST00000368378.3,ENST00000460050.1,ENST00000541990.1,ENST00000428962.2 |
| exon_skip_32259 | 1 | 155172883:155172928:155173013:155173096:155173303:155173330 | 155173013:155173096 | ENSG00000169231.9 | ENST00000486260.1,ENST00000457183.2,ENST00000368378.3,ENST00000541990.1 |
| exon_skip_32268 | 1 | 155173013:155173096:155173303:155173330:155174645:155174748 | 155173303:155173330 | ENSG00000169231.9 | ENST00000486260.1,ENST00000368378.3 |
| exon_skip_32269 | 1 | 155173013:155173096:155173303:155173330:155174850:155175107 | 155173303:155173330 | ENSG00000169231.9 | ENST00000541990.1 |
| exon_skip_32270 | 1 | 155173013:155173096:155173303:155173330:155175990:155176197 | 155173303:155173330 | ENSG00000169231.9 | ENST00000457183.2 |
| exon_skip_32277 | 1 | 155173303:155173330:155174645:155174748:155174850:155175054 | 155174645:155174748 | ENSG00000169231.9 | ENST00000486260.1,ENST00000368378.3 |
| exon_skip_32305 | 1 | 155174850:155175107:155175983:155176197:155177588:155177688 | 155175983:155176197 | ENSG00000169231.9 | ENST00000541990.1 |
| exon_skip_32309 | 1 | 155174850:155175107:155175990:155176197:155177588:155177688 | 155175990:155176197 | ENSG00000169231.9 | ENST00000368378.3 |
| Exon skip ID | chr | Exons involved in exon skipping | Skipped exon | ENSG | ENSTs |
| exon_skip_32244 | 1 | 155165635:155165690:155165777:155165917:155166831:155167000 | 155165777:155165917 | ENSG00000169231.9 | ENST00000368378.3,ENST00000541576.1,ENST00000457183.2,ENST00000541990.1,ENST00000469769.1 |
| exon_skip_32245 | 1 | 155166831:155167004:155167253:155167450:155167670:155167719 | 155167253:155167450 | ENSG00000169231.9 | ENST00000368378.3,ENST00000541576.1,ENST00000457183.2,ENST00000541990.1 |
| exon_skip_32249 | 1 | 155169785:155169904:155170241:155170401:155170687:155170795 | 155170241:155170401 | ENSG00000169231.9 | ENST00000368378.3,ENST00000541576.1,ENST00000457183.2,ENST00000541990.1 |
| exon_skip_32250 | 1 | 155170246:155170401:155170687:155170795:155170884:155170995 | 155170687:155170795 | ENSG00000169231.9 | ENST00000368378.3,ENST00000457183.2,ENST00000541990.1,ENST00000486260.1 |
| exon_skip_32251 | 1 | 155170246:155170401:155170687:155170795:155171207:155171360 | 155170687:155170795 | ENSG00000169231.9 | ENST00000541576.1 |
| exon_skip_32255 | 1 | 155170689:155170795:155170884:155170995:155171207:155171360 | 155170884:155170995 | ENSG00000169231.9 | ENST00000368378.3,ENST00000457183.2,ENST00000541990.1,ENST00000428962.2,ENST00000486260.1,ENST00000460050.1 |
| exon_skip_32259 | 1 | 155172883:155172928:155173013:155173096:155173303:155173330 | 155173013:155173096 | ENSG00000169231.9 | ENST00000368378.3,ENST00000457183.2,ENST00000541990.1,ENST00000486260.1 |
| exon_skip_32268 | 1 | 155173013:155173096:155173303:155173330:155174645:155174748 | 155173303:155173330 | ENSG00000169231.9 | ENST00000368378.3,ENST00000486260.1 |
| exon_skip_32269 | 1 | 155173013:155173096:155173303:155173330:155174850:155175107 | 155173303:155173330 | ENSG00000169231.9 | ENST00000541990.1 |
| exon_skip_32270 | 1 | 155173013:155173096:155173303:155173330:155175990:155176197 | 155173303:155173330 | ENSG00000169231.9 | ENST00000457183.2 |
| exon_skip_32277 | 1 | 155173303:155173330:155174645:155174748:155174850:155175054 | 155174645:155174748 | ENSG00000169231.9 | ENST00000368378.3,ENST00000486260.1 |
| exon_skip_32305 | 1 | 155174850:155175107:155175983:155176197:155177588:155177688 | 155175983:155176197 | ENSG00000169231.9 | ENST00000541990.1 |
| exon_skip_32309 | 1 | 155174850:155175107:155175990:155176197:155177588:155177688 | 155175990:155176197 | ENSG00000169231.9 | ENST00000368378.3 |
| 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 |
| P49746 | 26 | 95 | 23 | 956 | Chain | ID=PRO_0000035849;Note=Thrombospondin-3 |
| P49746 | 26 | 95 | 23 | 193 | Domain | Note=Laminin G-like |
| P49746 | 443 | 480 | 23 | 956 | Chain | ID=PRO_0000035849;Note=Thrombospondin-3 |
| P49746 | 443 | 480 | 444 | 455 | Disulfide bond | Ontology_term=ECO:0000255;evidence=ECO:0000255|PROSITE-ProRule:PRU00076 |
| P49746 | 443 | 480 | 471 | 478 | Disulfide bond | Ontology_term=ECO:0000255;evidence=ECO:0000255|PROSITE-ProRule:PRU00076 |
| P49746 | 443 | 480 | 414 | 456 | Domain | Note=EGF-like 3;Ontology_term=ECO:0000255;evidence=ECO:0000255|PROSITE-ProRule:PRU00076 |
| P49746 | 443 | 480 | 457 | 491 | Repeat | Note=TSP type-3 1 |
| P49746 | 480 | 516 | 23 | 956 | Chain | ID=PRO_0000035849;Note=Thrombospondin-3 |
| P49746 | 480 | 516 | 483 | 503 | Disulfide bond | Ontology_term=ECO:0000255;evidence=ECO:0000255|PROSITE-ProRule:PRU00076 |
| P49746 | 480 | 516 | 457 | 491 | Repeat | Note=TSP type-3 1 |
| P49746 | 480 | 516 | 492 | 527 | Repeat | Note=TSP type-3 2 |
| 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 |
| P49746 | 26 | 95 | 23 | 956 | Chain | ID=PRO_0000035849;Note=Thrombospondin-3 |
| P49746 | 26 | 95 | 23 | 193 | Domain | Note=Laminin G-like |
| P49746 | 443 | 480 | 23 | 956 | Chain | ID=PRO_0000035849;Note=Thrombospondin-3 |
| P49746 | 443 | 480 | 444 | 455 | Disulfide bond | Ontology_term=ECO:0000255;evidence=ECO:0000255|PROSITE-ProRule:PRU00076 |
| P49746 | 443 | 480 | 471 | 478 | Disulfide bond | Ontology_term=ECO:0000255;evidence=ECO:0000255|PROSITE-ProRule:PRU00076 |
| P49746 | 443 | 480 | 414 | 456 | Domain | Note=EGF-like 3;Ontology_term=ECO:0000255;evidence=ECO:0000255|PROSITE-ProRule:PRU00076 |
| P49746 | 443 | 480 | 457 | 491 | Repeat | Note=TSP type-3 1 |
| P49746 | 480 | 516 | 23 | 956 | Chain | ID=PRO_0000035849;Note=Thrombospondin-3 |
| P49746 | 480 | 516 | 483 | 503 | Disulfide bond | Ontology_term=ECO:0000255;evidence=ECO:0000255|PROSITE-ProRule:PRU00076 |
| P49746 | 480 | 516 | 457 | 491 | Repeat | Note=TSP type-3 1 |
| P49746 | 480 | 516 | 492 | 527 | Repeat | Note=TSP type-3 2 |
| Cancer type | Sample | ESID | Skipped exon start | Skipped exon end | Mutation start | Mutation end | Mutation type | Reference seq | Mutation seq | AAchange |
| LIHC | TCGA-DD-A1EG-01 | exon_skip_32244
| 155165778 | 155165917 | 155165845 | 155165845 | Frame_Shift_Del | C | - | p.G915fs |
| LIHC | TCGA-DD-A3A0-01 | exon_skip_32244
| 155165778 | 155165917 | 155165845 | 155165845 | Frame_Shift_Del | C | - | p.G915fs |
| LIHC | TCGA-DD-A4NA-01 | exon_skip_32250 exon_skip_32251
| 155170688 | 155170795 | 155170766 | 155170766 | Frame_Shift_Del | C | - | p.G490fs |
| LIHC | TCGA-DD-A4NA-01 | exon_skip_32250 exon_skip_32251
| 155170688 | 155170795 | 155170766 | 155170766 | Frame_Shift_Del | C | - | p.Q491fs |
| LIHC | TCGA-DD-A1EG-01 | exon_skip_32305 exon_skip_32309
| 155175984 | 155176197 | 155176079 | 155176079 | Frame_Shift_Del | G | - | p.P66fs |
| LIHC | TCGA-DD-A1EG-01 | exon_skip_32305 exon_skip_32309
| 155175991 | 155176197 | 155176079 | 155176079 | Frame_Shift_Del | G | - | p.P66fs |
| LIHC | TCGA-DD-A39Y-01 | exon_skip_32305 exon_skip_32309
| 155175984 | 155176197 | 155176079 | 155176079 | Frame_Shift_Del | G | - | p.P66fs |
| LIHC | TCGA-DD-A39Y-01 | exon_skip_32305 exon_skip_32309
| 155175991 | 155176197 | 155176079 | 155176079 | Frame_Shift_Del | G | - | p.P66fs |
| LIHC | TCGA-G3-A3CJ-01 | exon_skip_32305 exon_skip_32309
| 155175984 | 155176197 | 155176079 | 155176079 | Frame_Shift_Del | G | - | p.P66fs |
| LIHC | TCGA-G3-A3CJ-01 | exon_skip_32305 exon_skip_32309
| 155175991 | 155176197 | 155176079 | 155176079 | Frame_Shift_Del | G | - | p.P66fs |
| LIHC | TCGA-G3-A3CG-01 | exon_skip_32245
| 155167254 | 155167450 | 155167449 | 155167450 | Frame_Shift_Ins | - | A | p.G768fs |
| BLCA | TCGA-ZF-AA4X-01 | exon_skip_32244
| 155165778 | 155165917 | 155165787 | 155165787 | Nonsense_Mutation | G | A | p.R935* |
| LIHC | TCGA-G3-A3CG-01 | exon_skip_32245
| 155167254 | 155167450 | 155167451 | 155167451 | Splice_Site | C | T | . |
| STAD | TCGA-HF-A5NB-01 | exon_skip_32305 exon_skip_32309
| 155175991 | 155176197 | 155175989 | 155175989 | Splice_Site | A | G | . |
| Sample | Skipped exon start | Skipped exon end | Mutation start | Mutation end | Mutation type | Reference seq | Mutation seq | AAchange |
| MERO48A_LUNG | 155165778 | 155165917 | 155165845 | 155165845 | Frame_Shift_Del | C | - | p.G915fs |
| SNGM_ENDOMETRIUM | 155165778 | 155165917 | 155165845 | 155165845 | Frame_Shift_Del | C | - | p.G915fs |
| LS411N_LARGE_INTESTINE | 155165778 | 155165917 | 155165845 | 155165845 | Frame_Shift_Del | C | - | p.G915fs |
| MM1S_HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 155170242 | 155170401 | 155170259 | 155170263 | Frame_Shift_Del | TTGTC | - | p.DN563fs |
| CTV1_HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 155170242 | 155170401 | 155170278 | 155170278 | Frame_Shift_Del | C | - | p.E558fs |
| MDAPCA2B_PROSTATE | 155167254 | 155167450 | 155167268 | 155167268 | Missense_Mutation | C | T | p.G829R |
| UW228_CENTRAL_NERVOUS_SYSTEM | 155167254 | 155167450 | 155167286 | 155167286 | Missense_Mutation | G | A | p.R823W |
| HEC6_ENDOMETRIUM | 155167254 | 155167450 | 155167345 | 155167345 | Missense_Mutation | C | T | p.R803H |
| GI1_CENTRAL_NERVOUS_SYSTEM | 155167254 | 155167450 | 155167345 | 155167345 | Missense_Mutation | C | T | p.R803H |
| HEC50B_ENDOMETRIUM | 155167254 | 155167450 | 155167346 | 155167346 | Missense_Mutation | G | T | p.R803S |
| SNU520_STOMACH | 155167254 | 155167450 | 155167415 | 155167415 | Missense_Mutation | T | C | p.T780A |
| HCC202_BREAST | 155167254 | 155167450 | 155167430 | 155167430 | Missense_Mutation | C | T | p.V775M |
| LOVO_LARGE_INTESTINE | 155167254 | 155167450 | 155167432 | 155167432 | Missense_Mutation | C | T | p.G774D |
| NCC021_KIDNEY | 155170242 | 155170401 | 155170358 | 155170358 | Missense_Mutation | T | C | p.D531G |
| GP2D_LARGE_INTESTINE | 155170242 | 155170401 | 155170364 | 155170364 | Missense_Mutation | T | C | p.N529S |
| GP5D_LARGE_INTESTINE | 155170242 | 155170401 | 155170364 | 155170364 | Missense_Mutation | T | C | p.N529S |
| RPMI8402_HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 155170242 | 155170401 | 155170369 | 155170369 | Missense_Mutation | C | A | p.Q527H |
| MDAMB453_BREAST | 155170688 | 155170795 | 155170720 | 155170720 | Missense_Mutation | C | T | p.D506N |
| NCIH1930_LUNG | 155170688 | 155170795 | 155170791 | 155170791 | Missense_Mutation | T | G | p.N482T |
| REH_HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 155173014 | 155173096 | 155173019 | 155173019 | Missense_Mutation | C | T | p.D251N |
| CTV1_HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 155173014 | 155173096 | 155173021 | 155173021 | Missense_Mutation | C | T | p.R250Q |
| DND41_HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 155173014 | 155173096 | 155173061 | 155173061 | Missense_Mutation | G | T | p.L237I |
| BICR18_UPPER_AERODIGESTIVE_TRACT | 155173304 | 155173330 | 155173324 | 155173324 | Missense_Mutation | T | C | p.N218S |
| MOLT4_HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 155174646 | 155174748 | 155174679 | 155174679 | Missense_Mutation | G | A | p.P205S |
| MM415_SKIN | 155175984 | 155176197 | 155176044 | 155176044 | Missense_Mutation | C | T | p.R78H |
| MM415_SKIN | 155175991 | 155176197 | 155176044 | 155176044 | Missense_Mutation | C | T | p.R78H |
| JURKAT_HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 155175984 | 155176197 | 155176132 | 155176132 | Missense_Mutation | C | T | p.A49T |
| JURKAT_HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 155175991 | 155176197 | 155176132 | 155176132 | Missense_Mutation | C | T | p.A49T |
| NUGC3_STOMACH | 155175984 | 155176197 | 155176167 | 155176167 | Missense_Mutation | C | A | p.R37L |
| NUGC3_STOMACH | 155175991 | 155176197 | 155176167 | 155176167 | Missense_Mutation | C | A | p.R37L |
| ES7_BONE | 155173014 | 155173096 | 155173022 | 155173022 | Nonsense_Mutation | G | A | p.R250* |