Primary Site >> Liver Cancer
Gene >> CACNA1C
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000347598 |
| Start | 2608573:2608573(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3479T>A |
| AA Mutation | p.Val1160Glu(p.V1160E) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000347598 |
| Start | 2691075:2691075(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.6437T>A |
| AA Mutation | p.Val2146Glu(p.V2146E) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000347598 |
| Start | 2691144:2691144(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.6506G>T |
| AA Mutation | p.Gly2169Val(p.G2169V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000347598 |
| Start | 2504930:2504930(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1202T>C |
| AA Mutation | p.Leu401Pro(p.L401P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000347598 |
| Start | 2449111:2449111(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.613G>T |
| AA Mutation | p.Val205Leu(p.V205L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000347598 |
| Start | 2664872:2664872(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.4424C>T |
| AA Mutation | p.Pro1475Leu(p.P1475L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000347598 |
| Start | 2610571:2610571(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3649C>T |
| AA Mutation | p.Arg1217Trp(p.R1217W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000347598 |
| Start | 2679551:2679551(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs200638007 |
| CDS Mutation | c.5343G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |