Primary Site >> Liver Cancer
Gene >> CD109
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000287097 |
| Start | 73792782:73792782(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2858C>G |
| AA Mutation | p.Ala953Gly(p.A953G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000287097 |
| Start | 73792767:73792767(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2843A>C |
| AA Mutation | p.Asn948Thr(p.N948T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000287097 |
| Start | 73736431:73736431(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.556C>G |
| AA Mutation | p.Leu186Val(p.L186V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000287097 |
| Start | 73771433:73771433(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1679A>C |
| AA Mutation | p.Lys560Thr(p.K560T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000287097 |
| Start | 73697433:73697433(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs776339213 |
| CDS Mutation | c.108C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000287097 |
| Start | 73782650:73782650(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.2003delA |
| AA Mutation | p.Asn668MetfsTer6(p.N668Mfs*6) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |