Primary Site >> Esophagus Cancer
Gene >> CACNA1C
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000347598 |
| Start | 2567572:2567572(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs572234918 |
| CDS Mutation | c.1673C>T |
| AA Mutation | p.Thr558Met(p.T558M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000347598 |
| Start | 2691158:2691158(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.6520G>A |
| AA Mutation | p.Glu2174Lys(p.E2174K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000347598 |
| Start | 2674549:2674549(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.4879G>C |
| AA Mutation | p.Glu1627Gln(p.E1627Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000347598 |
| Start | 2584597:2584597(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2319G>T |
| AA Mutation | p.Lys773Asn(p.K773N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000347598 |
| Start | 2677856:2677856(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.5224G>A |
| AA Mutation | p.Asp1742Asn(p.D1742N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000347598 |
| Start | 2651723:2651723(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.4173G>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000347598 |
| Start | 2115342:2115342(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs763760402 |
| CDS Mutation | c.168C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000347598 |
| Start | 2549971:2549971(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs368065584 |
| CDS Mutation | c.1419C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000347598 |
| Start | 2581674:2581674(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1980C>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |