Primary Site >> Liver Cancer
Gene >> CACNA2D1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000356253 |
| Start | 81962011:81962011(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2885A>G |
| AA Mutation | p.Asp962Gly(p.D962G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000356253 |
| Start | 81964107:81964107(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2765C>T |
| AA Mutation | p.Pro922Leu(p.P922L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000356253 |
| Start | 81950465:81950465(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3239C>A |
| AA Mutation | p.Ser1080Tyr(p.S1080Y) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000356253 |
| Start | 82335247:82335247(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.182A>T |
| AA Mutation | p.Tyr61Phe(p.Y61F) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000356253 |
| Start | 81974542:81974542(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2002A>C |
| AA Mutation | p.Asn668His(p.N668H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000356253 |
| Start | 82084790:82084790(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.637G>T |
| AA Mutation | p.Gly213Cys(p.G213C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000356253 |
| Start | 81959806:81959806(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3026T>A |
| AA Mutation | p.Met1009Lys(p.M1009K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000356253 |
| Start | 82013505:82013505(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1228T>C |
| AA Mutation | p.Tyr410His(p.Y410H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000356253 |
| Start | 81961996:81961996(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2900C>A |
| AA Mutation | p.Ala967Asp(p.A967D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000356253 |
| Start | 82060490:82060490(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs754162606 |
| CDS Mutation | c.817C>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |