Primary Site >> Stomach Cancer
Gene >> BRIP1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000259008 |
| Start | 61857093:61857093(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.344C>A |
| AA Mutation | p.Pro115His(p.P115H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000259008 |
| Start | 61859865:61859865(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.136A>G |
| AA Mutation | p.Ser46Gly(p.S46G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000259008 |
| Start | 61686148:61686148(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs578022079 |
| CDS Mutation | c.2593C>T |
| AA Mutation | p.Arg865Trp(p.R865W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000259008 |
| Start | 61686049:61686049(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2692G>A |
| AA Mutation | p.Asp898Asn(p.D898N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000259008 |
| Start | 61683864:61683864(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3182A>G |
| AA Mutation | p.Asn1061Ser(p.N1061S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000259008 |
| Start | 61808517:61808517(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs145601931 |
| CDS Mutation | c.868G>A |
| AA Mutation | p.Gly290Ser(p.G290S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |