Primary Site >> Liver Cancer
Gene >> TRPC6
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000344327 |
| Start | 101504551:101504551(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.418G>T |
| AA Mutation | p.Ala140Ser(p.A140S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000344327 |
| Start | 101452958:101452958(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2793A>T |
| AA Mutation | p.Arg931Ser(p.R931S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000344327 |
| Start | 101504566:101504566(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.403A>T |
| AA Mutation | p.Asn135Tyr(p.N135Y) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000344327 |
| Start | 101504766:101504766(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs369866012 |
| CDS Mutation | c.203G>A |
| AA Mutation | p.Arg68Gln(p.R68Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000344327 |
| Start | 101473757:101473757(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs747089189 |
| CDS Mutation | c.1761C>A |
| AA Mutation | p.Asp587Glu(p.D587E) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000344327 |
| Start | 101453012:101453012(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs756864306 |
| CDS Mutation | c.2739T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000344327 |
| Start | 101504482:101504482(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.487delG |
| AA Mutation | p.Asp163MetfsTer5(p.D163Mfs*5) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000344327 |
| Start | 101504275:101504275(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.694delT |
| AA Mutation | p.Tyr232MetfsTer64(p.Y232Mfs*64) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |