Primary Site >> Stomach Cancer
Gene >> TUFT1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000368849 |
| Start | 151581691:151581691(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs368431369 |
| CDS Mutation | c.1157G>A |
| AA Mutation | p.Arg386Gln(p.R386Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000368849 |
| Start | 151574286:151574286(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.611A>G |
| AA Mutation | p.Tyr204Cys(p.Y204C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000368849 |
| Start | 151566200:151566200(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.452C>A |
| AA Mutation | p.Pro151His(p.P151H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000368849 |
| Start | 151574279:151574279(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.604A>G |
| AA Mutation | p.Ser202Gly(p.S202G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000368849 |
| Start | 151563984:151563984(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.318C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000368849 |
| Start | 151580960:151580960(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1027C>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000368849 |
| Start | 151579684:151579684(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs746150897 |
| CDS Mutation | c.960C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |