Primary Site >> Stomach Cancer
Gene >> TAS2R7
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000240687 |
| Start | 10802279:10802279(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.292T>C |
| AA Mutation | p.Trp98Arg(p.W98R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000240687 |
| Start | 10802095:10802095(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.476G>T |
| AA Mutation | p.Cys159Phe(p.C159F) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000240687 |
| Start | 10801930:10801930(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs757204228 |
| CDS Mutation | c.641G>A |
| AA Mutation | p.Arg214Gln(p.R214Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000240687 |
| Start | 10802199:10802199(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.372G>C |
| AA Mutation | p.Trp124Cys(p.W124C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000240687 |
| Start | 10802160:10802160(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs375435543 |
| CDS Mutation | c.411C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000240687 |
| Start | 10801956:10801956(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs751352517 |
| CDS Mutation | c.615C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |