Primary Site >> Liver Cancer
Gene >> CAMTA1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000303635 |
| Start | 7738111:7738111(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3811A>C |
| AA Mutation | p.Asn1271His(p.N1271H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000303635 |
| Start | 7736460:7736460(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3183G>C |
| AA Mutation | p.Lys1061Asn(p.K1061N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000303635 |
| Start | 7737363:7737363(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3451G>A |
| AA Mutation | p.Ala1151Thr(p.A1151T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000303635 |
| Start | 7661861:7661861(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs761165547 |
| CDS Mutation | c.800G>C |
| AA Mutation | p.Ser267Thr(p.S267T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000303635 |
| Start | 7664303:7664303(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1756T>G |
| AA Mutation | p.Phe586Val(p.F586V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000303635 |
| Start | 7664632:7664632(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2085G>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000303635 |
| Start | 7640405:7640405(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs775725704 |
| CDS Mutation | c.516C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |