Primary Site >> Esophagus Cancer
Gene >> MUC4
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000463781 |
| Start | 195781429:195781429(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs201335957 |
| CDS Mutation | c.10151C>T |
| AA Mutation | p.Ser3384Leu(p.S3384L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000463781 |
| Start | 195791032:195791032(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.548C>A |
| AA Mutation | p.Ser183Tyr(p.S183Y) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000463781 |
| Start | 195788627:195788627(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2953G>A |
| AA Mutation | p.Ala985Thr(p.A985T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000463781 |
| Start | 195782638:195782638(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.8942A>T |
| AA Mutation | p.Asp2981Val(p.D2981V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000463781 |
| Start | 195788510:195788510(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs369312980 |
| CDS Mutation | c.3070C>T |
| AA Mutation | p.Pro1024Ser(p.P1024S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000463781 |
| Start | 195754299:195754299(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.15242C>T |
| AA Mutation | p.Pro5081Leu(p.P5081L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000463781 |
| Start | 195782209:195782209(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs200289412 |
| CDS Mutation | c.9371C>G |
| AA Mutation | p.Thr3124Ser(p.T3124S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000463781 |
| Start | 195783871:195783871(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.7709C>T |
| AA Mutation | p.Ser2570Phe(p.S2570F) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000463781 |
| Start | 195783079:195783079(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.8501C>T |
| AA Mutation | p.Pro2834Leu(p.P2834L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000463781 |
| Start | 195791167:195791167(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.413T>C |
| AA Mutation | p.Ile138Thr(p.I138T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000463781 |
| Start | 195778443:195778443(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs142178516 |
| CDS Mutation | c.12803C>T |
| AA Mutation | p.Pro4268Leu(p.P4268L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000463781 |
| Start | 195779975:195779975(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.11605C>T |
| AA Mutation | p.His3869Tyr(p.H3869Y) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000463781 |
| Start | 195782737:195782737(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.8843C>T |
| AA Mutation | p.Thr2948Ile(p.T2948I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000463781 |
| Start | 195782175:195782175(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs769389598 |
| CDS Mutation | c.9405C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000463781 |
| Start | 195782163:195782163(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.9417C>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000463781 |
| Start | 195783957:195783957(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs761000297 |
| CDS Mutation | c.7623C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 17 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000463781 |
| Start | 195784710:195784710(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.6870T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 18 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000463781 |
| Start | 195747281:195747281(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs199920657 |
| CDS Mutation | c.16134C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 19 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000463781 |
| Start | 195785797:195785797(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.5783C>G |
| AA Mutation | p.Ser1928Ter(p.S1928*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |
| ID | 20 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000463781 |
| Start | 195785132:195785133(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | novel |
| CDS Mutation | c.6447_6448insC |
| AA Mutation | p.Thr2150HisfsTer104(p.T2150Hfs*104) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |
| ID | 21 |
| Mutation Consequence | inframe_insertion |
| Transcription ID | ENST00000463781 |
| Start | 195780992:195780993(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | novel |
| CDS Mutation | c.10587_10588insCCCACAGGTCACGCCACCCCTCTTCCTGTCACCAGCTTTTCCTCAGTATCCACAGGTGACACCACCCCTCTTCCTGTCACCGACGCTTCCTCGGCATCCACCGGTCACGCCACCCCTCTTCCTGTCACCGACACTTCCTCAGTA |
| AA Mutation | p.Val3529_Ser3530insProThrGlyHisAlaThrProLeuProValThrSerPheSerSerValSerThrGlyAspThrThrProLeuProValThrAspAlaSerSerAlaSerThrGlyHisAlaThrProLeuProValThrAspThrSerSerVal(p.V3529_S3530insPTGHATPLPVTSFSSVSTGDTTPLPVTDASSASTGHATPLPVTDTSSV) |
| Mutation Classification | In_Frame_Ins |
| Feature Type | Transcript |
| ID | 22 |
| Mutation Consequence | inframe_insertion |
| Transcription ID | ENST00000463781 |
| Start | 195783009:195783010(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | novel |
| CDS Mutation | c.8570_8571insACCCACAGGTCACGCCTCCTCTCTTCCTGTCACCGACGCTTCCTCAGT |
| AA Mutation | p.Val2857_Ser2858insProThrGlyHisAlaSerSerLeuProValThrAspAlaSerSerVal(p.V2857_S2858insPTGHASSLPVTDASSV) |
| Mutation Classification | In_Frame_Ins |
| Feature Type | Transcript |