Primary Site >> Liver Cancer
Gene >> CHD4
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000357008 |
| Start | 6591986:6591986(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3020C>T |
| AA Mutation | p.Ser1007Phe(p.S1007F) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000357008 |
| Start | 6581726:6581726(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.4604C>T |
| AA Mutation | p.Ser1535Leu(p.S1535L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000357008 |
| Start | 6592698:6592698(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2772C>G |
| AA Mutation | p.Phe924Leu(p.F924L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000357008 |
| Start | 6583338:6583338(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3920A>G |
| AA Mutation | p.Glu1307Gly(p.E1307G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000357008 |
| Start | 6601399:6601399(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.689C>T |
| AA Mutation | p.Ala230Val(p.A230V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000357008 |
| Start | 6573128:6573128(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs778830438 |
| CDS Mutation | c.5503C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000357008 |
| Start | 6594600:6594612(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.2160_2172delTGCTACAGGTGGA |
| AA Mutation | p.Asp720GlufsTer11(p.D720Efs*11) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000357008 |
| Start | 6601697:6601697(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.508G>T |
| AA Mutation | p.Glu170Ter(p.E170*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |