Primary Site >> Stomach Cancer
Gene >> GPI
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000356487 |
| Start | 34396389:34396389(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1151G>T |
| AA Mutation | p.Gly384Val(p.G384V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000356487 |
| Start | 34377564:34377564(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.464T>G |
| AA Mutation | p.Ile155Ser(p.I155S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000356487 |
| Start | 34399631:34399631(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs773208058 |
| CDS Mutation | c.1474G>A |
| AA Mutation | p.Ala492Thr(p.A492T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000356487 |
| Start | 34396325:34396325(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1087T>C |
| AA Mutation | p.Tyr363His(p.Y363H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000356487 |
| Start | 34377873:34377873(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.625G>A |
| AA Mutation | p.Ala209Thr(p.A209T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000356487 |
| Start | 34366797:34366797(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs150838903 |
| CDS Mutation | c.228C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000356487 |
| Start | 34399991:34399991(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs376737076 |
| CDS Mutation | c.1632G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |