Primary Site >> Stomach Cancer
Gene >> IRF3
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000309877 |
| Start | 49663415:49663415(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs369809017 |
| CDS Mutation | c.265G>A |
| AA Mutation | p.Gly89Arg(p.G89R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000309877 |
| Start | 49662104:49662104(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs566321486 |
| CDS Mutation | c.826C>T |
| AA Mutation | p.Arg276Trp(p.R276W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000309877 |
| Start | 49663474:49663474(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.206A>G |
| AA Mutation | p.Asp69Gly(p.D69G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000309877 |
| Start | 49662261:49662261(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs778251209 |
| CDS Mutation | c.669G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000309877 |
| Start | 49659750:49659750(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1182C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000309877 |
| Start | 49663437:49663437(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.243C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000309877 |
| Start | 49662219:49662219(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs376377408 |
| CDS Mutation | c.711G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |