Primary Site >> Stomach Cancer
Gene >> BIRC7
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000217169 |
| Start | 63237987:63237987(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs752843916 |
| CDS Mutation | c.434C>A |
| AA Mutation | p.Ala145Asp(p.A145D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000217169 |
| Start | 63238600:63238600(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.563C>A |
| AA Mutation | p.Pro188His(p.P188H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000217169 |
| Start | 63239589:63239589(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs142521563 |
| CDS Mutation | c.881G>A |
| AA Mutation | p.Arg294His(p.R294H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000217169 |
| Start | 63239583:63239583(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.875G>C |
| AA Mutation | p.Arg292Pro(p.R292P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000217169 |
| Start | 63239535:63239535(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.827C>T |
| AA Mutation | p.Ala276Val(p.A276V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000217169 |
| Start | 63237967:63237967(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs776404641 |
| CDS Mutation | c.414C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000217169 |
| Start | 63237938:63237938(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.389delG |
| AA Mutation | p.Gly130AlafsTer233(p.G130Afs*233) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |