Primary Site >> Stomach Cancer
Gene >> FOXO1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000379561 |
| Start | 40560817:40560817(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.674G>A |
| AA Mutation | p.Arg225His(p.R225H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000379561 |
| Start | 40560268:40560268(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs772929365 |
| CDS Mutation | c.1223C>T |
| AA Mutation | p.Ala408Val(p.A408V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000379561 |
| Start | 40560712:40560712(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.779A>G |
| AA Mutation | p.Asn260Ser(p.N260S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000379561 |
| Start | 40560818:40560818(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.673C>T |
| AA Mutation | p.Arg225Cys(p.R225C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000379561 |
| Start | 40559998:40559998(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1493T>C |
| AA Mutation | p.Met498Thr(p.M498T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000379561 |
| Start | 40560273:40560273(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1218G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000379561 |
| Start | 40560111:40560111(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1380A>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000379561 |
| Start | 40560387:40560387(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs752627269 |
| CDS Mutation | c.1104C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000379561 |
| Start | 40560117:40560117(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs555035704 |
| CDS Mutation | c.1374G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |