Primary Site >> Liver Cancer
Gene >> ZNF135
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000313434 |
| Start | 58067545:58067545(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1061A>T |
| AA Mutation | p.Tyr354Phe(p.Y354F) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000313434 |
| Start | 58067980:58067980(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1496G>A |
| AA Mutation | p.Cys499Tyr(p.C499Y) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000313434 |
| Start | 58067082:58067082(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.598G>C |
| AA Mutation | p.Asp200His(p.D200H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000313434 |
| Start | 58063486:58063486(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.201G>T |
| AA Mutation | p.Glu67Asp(p.E67D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000313434 |
| Start | 58067775:58067775(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1291A>G |
| AA Mutation | p.Ile431Val(p.I431V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000313434 |
| Start | 58067730:58067730(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1246G>A |
| AA Mutation | p.Gly416Arg(p.G416R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000313434 |
| Start | 58067982:58067982(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs566725358 |
| CDS Mutation | c.1498G>A |
| AA Mutation | p.Gly500Ser(p.G500S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000313434 |
| Start | 58060029:58060029(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs777966791 |
| CDS Mutation | c.27A>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |