Primary Site >> Stomach Cancer
Gene >> F2
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000311907 |
| Start | 46729544:46729544(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1637A>G |
| AA Mutation | p.Asp546Gly(p.D546G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000311907 |
| Start | 46728732:46728732(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs143498218 |
| CDS Mutation | c.1367G>A |
| AA Mutation | p.Arg456Gln(p.R456Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000311907 |
| Start | 46725900:46725900(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.601G>T |
| AA Mutation | p.Gly201Cys(p.G201C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000311907 |
| Start | 46739272:46739272(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1733T>G |
| AA Mutation | p.Phe578Cys(p.F578C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000311907 |
| Start | 46729535:46729535(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs143064939 |
| CDS Mutation | c.1628G>A |
| AA Mutation | p.Arg543His(p.R543H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000311907 |
| Start | 46739102:46739102(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1709G>C |
| AA Mutation | p.Gly570Ala(p.G570A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000311907 |
| Start | 46723431:46723431(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs768825889 |
| CDS Mutation | c.472C>T |
| AA Mutation | p.Arg158Cys(p.R158C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000311907 |
| Start | 46728139:46728139(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs121918485 |
| CDS Mutation | c.1274G>A |
| AA Mutation | p.Arg425His(p.R425H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000311907 |
| Start | 46729415:46729415(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1508G>C |
| AA Mutation | p.Gly503Ala(p.G503A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000311907 |
| Start | 46726077:46726077(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.778A>T |
| AA Mutation | p.Asn260Tyr(p.N260Y) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000311907 |
| Start | 46719776:46719776(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.154C>T |
| AA Mutation | p.Arg52Cys(p.R52C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000311907 |
| Start | 46726017:46726017(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.718G>T |
| AA Mutation | p.Ala240Ser(p.A240S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000311907 |
| Start | 46726556:46726556(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs377529931 |
| CDS Mutation | c.933C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000311907 |
| Start | 46719278:46719278(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.43C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000311907 |
| Start | 46719241:46719241(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs748368751 |
| CDS Mutation | c.6G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |