Primary Site >> Liver Cancer
Gene >> MSH6
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000234420 |
| Start | 47799908:47799908(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1925A>G |
| AA Mutation | p.Tyr642Cys(p.Y642C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000234420 |
| Start | 47800156:47800156(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs148898662 |
| CDS Mutation | c.2173A>G |
| AA Mutation | p.Ile725Val(p.I725V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000234420 |
| Start | 47783390:47783405(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.158_173delCTGGGCCTGGGCCCAG |
| AA Mutation | p.Ala53GlyfsTer23(p.A53Gfs*23) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000234420 |
| Start | 47791099:47791099(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.433A>T |
| AA Mutation | p.Lys145Ter(p.K145*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |