Primary Site >> Stomach Cancer
Gene >> SLC16A7
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000261187 |
| Start | 59779626:59779626(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1384G>A |
| AA Mutation | p.Val462Ile(p.V462I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000261187 |
| Start | 59774731:59774731(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.436G>A |
| AA Mutation | p.Ala146Thr(p.A146T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000261187 |
| Start | 59704888:59704888(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.87C>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000261187 |
| Start | 59774685:59774685(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs201840996 |
| CDS Mutation | c.390C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000261187 |
| Start | 59775331:59775331(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | null |
| CDS Mutation | c.1041delT |
| AA Mutation | p.Phe347LeufsTer53(p.F347Lfs*53) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000261187 |
| Start | 59775223:59775223(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs769714200 |
| CDS Mutation | c.928C>T |
| AA Mutation | p.Arg310Ter(p.R310*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |