Primary Site >> Stomach Cancer
Gene >> GFAP
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000253408 |
| Start | 44911722:44911722(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs373831531 |
| CDS Mutation | c.856C>T |
| AA Mutation | p.Arg286Trp(p.R286W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000253408 |
| Start | 44915225:44915225(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs61622935 |
| CDS Mutation | c.262C>T |
| AA Mutation | p.Arg88Cys(p.R88C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000253408 |
| Start | 44915399:44915399(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs770249831 |
| CDS Mutation | c.88C>T |
| AA Mutation | p.Arg30Cys(p.R30C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000253408 |
| Start | 44915373:44915373(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.114C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000253408 |
| Start | 44915145:44915145(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs115282391 |
| CDS Mutation | c.342C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000253408 |
| Start | 44915199:44915199(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs779815330 |
| CDS Mutation | c.288G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |