Primary Site >> Stomach Cancer
Gene >> ABCG8
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000272286 |
| Start | 43872071:43872071(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1060C>T |
| AA Mutation | p.Arg354Cys(p.R354C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000272286 |
| Start | 43851715:43851715(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs762452685 |
| CDS Mutation | c.454C>T |
| AA Mutation | p.Arg152Cys(p.R152C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000272286 |
| Start | 43852791:43852791(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs764334802 |
| CDS Mutation | c.887C>T |
| AA Mutation | p.Ala296Val(p.A296V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000272286 |
| Start | 43874422:43874422(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1427C>T |
| AA Mutation | p.Ala476Val(p.A476V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000272286 |
| Start | 43877593:43877593(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs776778929 |
| CDS Mutation | c.1789C>T |
| AA Mutation | p.Arg597Trp(p.R597W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000272286 |
| Start | 43875353:43875353(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1696C>A |
| AA Mutation | p.Leu566Ile(p.L566I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000272286 |
| Start | 43852402:43852402(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs775624442 |
| CDS Mutation | c.610C>T |
| AA Mutation | p.Arg204Cys(p.R204C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000272286 |
| Start | 43872227:43872227(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1132G>A |
| AA Mutation | p.Val378Met(p.V378M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000272286 |
| Start | 43852825:43852825(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs780422381 |
| CDS Mutation | c.921C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000272286 |
| Start | 43851633:43851633(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs201431593 |
| CDS Mutation | c.372C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000272286 |
| Start | 43873841:43873841(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs567600982 |
| CDS Mutation | c.1266G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |