Primary Site >> Biliary tract Cancer
Gene >> MUC16
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000397910 |
| Start | 8937087:8937087(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.33868G>T |
| AA Mutation | p.Asp11290Tyr(p.D11290Y) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000397910 |
| Start | 8948077:8948077(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.28693C>T |
| AA Mutation | p.Pro9565Ser(p.P9565S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000397910 |
| Start | 8959644:8959644(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.17126C>G |
| AA Mutation | p.Ala5709Gly(p.A5709G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000397910 |
| Start | 8978978:8978978(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2161A>G |
| AA Mutation | p.Ser721Gly(p.S721G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000397910 |
| Start | 8962284:8962284(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.14486A>G |
| AA Mutation | p.Asn4829Ser(p.N4829S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000397910 |
| Start | 8961243:8961243(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.15527A>G |
| AA Mutation | p.Glu5176Gly(p.E5176G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000397910 |
| Start | 8959643:8959643(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.17127delC |
| AA Mutation | p.Met5710CysfsTer71(p.M5710Cfs*71) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000397910 |
| Start | 8957949:8957949(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.18821delG |
| AA Mutation | p.Arg6274LeufsTer6(p.R6274Lfs*6) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | stop_gained;frameshift_variant |
| Transcription ID | ENST00000397910 |
| Start | 8945871:8945872(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | novel |
| CDS Mutation | c.30898_30899insAATGGACTACCTGAACC |
| AA Mutation | p.Gly10300GlufsTer5(p.G10300Efs*5) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000397910 |
| Start | 8945873:8945874(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | novel |
| CDS Mutation | c.30896_30897insTGTCCTAG |
| AA Mutation | p.Gly10300ValfsTer55(p.G10300Vfs*55) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |