Exon skip ID | chr | Exons involved in exon skipping | Skipped exon | ENSG | ENSTs |
exon_skip_105210 | 14 | 23341512:23341546:23341946:23341991:23342519:23342655 | 23341946:23341991 | ENSG00000197324.4 | ENST00000546834.1 |
exon_skip_105212 | 14 | 23341946:23341991:23342519:23342655:23344263:23344454 | 23342519:23342655 | ENSG00000197324.4 | ENST00000546834.1,ENST00000359591.4 |
exon_skip_105214 | 14 | 23342519:23342655:23344263:23344454:23344563:23344674 | 23344263:23344454 | ENSG00000197324.4 | ENST00000553002.1,ENST00000546834.1,ENST00000359591.4 |
exon_skip_105230 | 14 | 23344344:23344454:23344563:23345581:23345897:23346027 | 23344563:23345581 | ENSG00000197324.4 | ENST00000551466.1,ENST00000546834.1,ENST00000359591.4 |
exon_skip_105249 | 14 | 23345477:23345581:23345897:23346027:23346148:23346262 | 23345897:23346027 | ENSG00000197324.4 | ENST00000551466.1,ENST00000546834.1,ENST00000359591.4 |
exon_skip_105254 | 14 | 23346184:23346262:23346635:23346805:23347192:23347252 | 23346635:23346805 | ENSG00000197324.4 | ENST00000470660.1 |
Exon skip ID | chr | Exons involved in exon skipping | Skipped exon | ENSG | ENSTs |
exon_skip_105210 | 14 | 23341512:23341546:23341946:23341991:23342519:23342655 | 23341946:23341991 | ENSG00000197324.4 | ENST00000546834.1 |
exon_skip_105212 | 14 | 23341946:23341991:23342519:23342655:23344263:23344454 | 23342519:23342655 | ENSG00000197324.4 | ENST00000359591.4,ENST00000546834.1 |
exon_skip_105214 | 14 | 23342519:23342655:23344263:23344454:23344563:23344674 | 23344263:23344454 | ENSG00000197324.4 | ENST00000359591.4,ENST00000546834.1,ENST00000553002.1 |
exon_skip_105230 | 14 | 23344344:23344454:23344563:23345581:23345897:23346027 | 23344563:23345581 | ENSG00000197324.4 | ENST00000359591.4,ENST00000546834.1,ENST00000551466.1 |
exon_skip_105249 | 14 | 23345477:23345581:23345897:23346027:23346148:23346262 | 23345897:23346027 | ENSG00000197324.4 | ENST00000359591.4,ENST00000546834.1,ENST00000551466.1 |
exon_skip_105254 | 14 | 23346184:23346262:23346635:23346805:23347192:23347252 | 23346635:23346805 | ENSG00000197324.4 | ENST00000470660.1 |
Depth of coverage in three exons | Mutation description |
| Sample: TCGA-55-8096-01 |
Cancer type: LUAD |
ESID: exon_skip_105230 |
Skipped exon start: 23344564 |
Skipped exon end: 23345581 |
Mutation start: 23345405 |
Mutation end: 23345405 |
Mutation type: Nonsense_Mutation |
Reference seq: G |
Mutation seq: A |
AAchange: p.W416* |
exon_skip_105230_LUAD_TCGA-55-8096-01.png
|
exon_skip_286364_LUAD_TCGA-55-8096-01.png
|
| Sample: TCGA-EL-A3ZR-01 |
Cancer type: THCA |
ESID: exon_skip_105230 |
Skipped exon start: 23344564 |
Skipped exon end: 23345581 |
Mutation start: 23345001 |
Mutation end: 23345001 |
Mutation type: Nonsense_Mutation |
Reference seq: C |
Mutation seq: T |
AAchange: p.Q282X |
| Sample: TCGA-EL-A3ZR-01 |
Cancer type: THCA |
ESID: exon_skip_105230 |
Skipped exon start: 23344564 |
Skipped exon end: 23345581 |
Mutation start: 23345001 |
Mutation end: 23345001 |
Mutation type: Nonsense_Mutation |
Reference seq: C |
Mutation seq: T |
AAchange: p.Q282* |
exon_skip_105230_THCA_TCGA-EL-A3ZR-01.png
|
Sample | Skipped exon start | Skipped exon end | Mutation start | Mutation end | Mutation type | Reference seq | Mutation seq | AAchange |
JURKAT_HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 23342520 | 23342655 | 23342530 | 23342530 | Frame_Shift_Del | C | - | p.D30fs |
RH18_SOFT_TISSUE | 23344564 | 23345581 | 23345154 | 23345155 | Frame_Shift_Del | AG | - | p.S333fs |
DG75_HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 23345898 | 23346027 | 23345906 | 23345906 | Frame_Shift_Del | C | - | p.A478fs |
REH_HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 23344564 | 23345581 | 23344689 | 23344690 | Frame_Shift_Ins | - | CCTT | p.-179fs |
NCIBL2009_MATCHED_NORMAL_TISSUE | 23341947 | 23341991 | 23341956 | 23341956 | Missense_Mutation | T | C | p.L15P |
UBLC1_URINARY_TRACT | 23341947 | 23341991 | 23341989 | 23341989 | Missense_Mutation | A | G | p.H26R |
KURAMOCHI_OVARY | 23342520 | 23342655 | 23342597 | 23342597 | Missense_Mutation | T | A | p.S53T |
MOLT3_HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 23342520 | 23342655 | 23342618 | 23342618 | Missense_Mutation | C | A | p.L60I |
MOLT4_HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 23342520 | 23342655 | 23342618 | 23342618 | Missense_Mutation | C | A | p.L60I |
UMUC1_URINARY_TRACT | 23344264 | 23344454 | 23344307 | 23344307 | Missense_Mutation | C | G | p.L87V |
CAL54_KIDNEY | 23344264 | 23344454 | 23344310 | 23344310 | Missense_Mutation | C | T | p.R88C |
NCIH1385_LUNG | 23344264 | 23344454 | 23344365 | 23344365 | Missense_Mutation | A | T | p.Q106L |
GSS_STOMACH | 23344264 | 23344454 | 23344380 | 23344380 | Missense_Mutation | A | G | p.N111S |
NCIH1915_LUNG | 23344564 | 23345581 | 23344608 | 23344608 | Missense_Mutation | C | T | p.R151C |
REH_HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 23344564 | 23345581 | 23344611 | 23344611 | Missense_Mutation | T | C | p.C152R |
SW48_LARGE_INTESTINE | 23344564 | 23345581 | 23344638 | 23344638 | Missense_Mutation | G | A | p.G161R |
MM426_SKIN | 23344564 | 23345581 | 23344660 | 23344660 | Missense_Mutation | G | A | p.G168D |
SNUC4_LARGE_INTESTINE | 23344564 | 23345581 | 23344716 | 23344716 | Missense_Mutation | G | A | p.V187I |
MEWO_SKIN | 23344564 | 23345581 | 23344720 | 23344720 | Missense_Mutation | C | T | p.P188L |
HKA1_SKIN | 23344564 | 23345581 | 23344801 | 23344801 | Missense_Mutation | C | T | p.S215F |
KARPAS422_HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 23344564 | 23345581 | 23344849 | 23344849 | Missense_Mutation | G | A | p.R231Q |
RERFLCAD2_LUNG | 23344564 | 23345581 | 23344945 | 23344945 | Missense_Mutation | G | T | p.R263L |
WM88_SKIN | 23344564 | 23345581 | 23345043 | 23345043 | Missense_Mutation | C | T | p.R296C |
HEC6_ENDOMETRIUM | 23344564 | 23345581 | 23345092 | 23345092 | Missense_Mutation | A | G | p.D312G |
HEC265_ENDOMETRIUM | 23344564 | 23345581 | 23345290 | 23345290 | Missense_Mutation | C | T | p.A378V |
HS742T_FIBROBLAST | 23344564 | 23345581 | 23345371 | 23345371 | Missense_Mutation | G | A | p.R405Q |
DOV13_OVARY | 23344564 | 23345581 | 23345424 | 23345424 | Missense_Mutation | G | T | p.D423Y |
2313287_STOMACH | 23344564 | 23345581 | 23345472 | 23345472 | Missense_Mutation | C | T | p.R439C |
CW2_LARGE_INTESTINE | 23344564 | 23345581 | 23345476 | 23345476 | Missense_Mutation | A | G | p.K440R |
COLO741_SKIN | 23344564 | 23345581 | 23345493 | 23345493 | Missense_Mutation | G | C | p.V446L |
HEC151_ENDOMETRIUM | 23345898 | 23346027 | 23345918 | 23345918 | Missense_Mutation | G | A | p.R482Q |
MUTZ5_HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 23345898 | 23346027 | 23345918 | 23345918 | Missense_Mutation | G | A | p.R482Q |
DOV13_OVARY | 23345898 | 23346027 | 23345920 | 23345920 | Missense_Mutation | A | C | p.M483L |
C4I_CERVIX | 23345898 | 23346027 | 23345963 | 23345963 | Missense_Mutation | G | A | p.G497E |
NB14_AUTONOMIC_GANGLIA | 23345898 | 23346027 | 23346019 | 23346019 | Missense_Mutation | C | A | p.P516T |
HEC59_ENDOMETRIUM | 23346636 | 23346805 | 23346711 | 23346711 | Missense_Mutation | C | T | p.A706V |
M14_SKIN | 23344564 | 23345581 | 23344626 | 23344626 | Nonsense_Mutation | C | T | p.Q157* |
MDAMB435S_SKIN | 23344564 | 23345581 | 23344626 | 23344626 | Nonsense_Mutation | C | T | p.Q157* |
SNUC4_LARGE_INTESTINE | 23342520 | 23342655 | 23342521 | 23342521 | Splice_Site | T | G | p.A27A |