Primary Site >> Stomach Cancer
Gene >> TKT
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000423525 |
| Start | 53255870:53255870(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs782431137 |
| CDS Mutation | c.73A>G |
| AA Mutation | p.Ser25Gly(p.S25G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000423525 |
| Start | 53231509:53231509(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs782480479 |
| CDS Mutation | c.790A>C |
| AA Mutation | p.Lys264Gln(p.K264Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000423525 |
| Start | 53229018:53229018(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs781856744 |
| CDS Mutation | c.1384G>A |
| AA Mutation | p.Ala462Thr(p.A462T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000423525 |
| Start | 53240273:53240273(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs782694913 |
| CDS Mutation | c.415G>A |
| AA Mutation | p.Gly139Ser(p.G139S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000423525 |
| Start | 53231495:53231495(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.804G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000423525 |
| Start | 53241186:53241186(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs140341715 |
| CDS Mutation | c.285G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |