Primary Site >> Stomach Cancer
Gene >> CYP26B1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000001146 |
| Start | 72133139:72133139(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs144968323 |
| CDS Mutation | c.1030C>T |
| AA Mutation | p.Arg344Cys(p.R344C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000001146 |
| Start | 72133058:72133058(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1111G>A |
| AA Mutation | p.Gly371Ser(p.G371S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000001146 |
| Start | 72133224:72133224(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.945C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000001146 |
| Start | 72132557:72132557(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs555351236 |
| CDS Mutation | c.1209G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000001146 |
| Start | 72144133:72144133(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.285C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000001146 |
| Start | 72144121:72144121(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs775445736 |
| CDS Mutation | c.297G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000001146 |
| Start | 72133164:72133164(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs148988710 |
| CDS Mutation | c.1005C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |