Primary Site >> Liver Cancer
Gene >> TAS1R1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000333172 |
| Start | 6575304:6575304(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs767318686 |
| CDS Mutation | c.1172G>A |
| AA Mutation | p.Arg391Gln(p.R391Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000333172 |
| Start | 6570923:6570923(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.206A>T |
| AA Mutation | p.Asn69Ile(p.N69I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000333172 |
| Start | 6579125:6579125(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2067C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000333172 |
| Start | 6571062:6571062(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs375985047 |
| CDS Mutation | c.345G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000333172 |
| Start | 6571119:6571119(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.402C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000333172 |
| Start | 6575375:6575375(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs772335281 |
| CDS Mutation | c.1243C>T |
| AA Mutation | p.Arg415Ter(p.R415*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |