Primary Site >> Stomach Cancer
Gene >> SLC25A6
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000381401 |
| Start | 1386678:1386678(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs778134725 |
| CDS Mutation | c.821C>T |
| AA Mutation | p.Ala274Val(p.A274V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000381401 |
| Start | 1389593:1389593(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.246C>A |
| AA Mutation | p.Phe82Leu(p.F82L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000381401 |
| Start | 1389522:1389522(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.317A>G |
| AA Mutation | p.His106Arg(p.H106R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000381401 |
| Start | 1386661:1386661(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.838C>T |
| AA Mutation | p.Arg280Trp(p.R280W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000381401 |
| Start | 1387310:1387310(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.708G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000381401 |
| Start | 1389518:1389518(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs561919681 |
| CDS Mutation | c.321G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |