Primary Site >> Stomach Cancer
Gene >> SLC19A1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000311124 |
| Start | 45515897:45515897(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1537C>T |
| AA Mutation | p.Pro513Ser(p.P513S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000311124 |
| Start | 45532060:45532060(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.278C>T |
| AA Mutation | p.Thr93Met(p.T93M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000311124 |
| Start | 45531882:45531882(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.456G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000311124 |
| Start | 45530955:45530955(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs776729245 |
| CDS Mutation | c.966C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000311124 |
| Start | 45531857:45531857(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.481C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000311124 |
| Start | 45525910:45525910(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs149270420 |
| CDS Mutation | c.1200C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |