Primary Site >> Stomach Cancer
Gene >> FBP2
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000375337 |
| Start | 94587444:94587444(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs777645239 |
| CDS Mutation | c.196G>A |
| AA Mutation | p.Val66Met(p.V66M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000375337 |
| Start | 94563403:94563403(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs550526190 |
| CDS Mutation | c.764G>A |
| AA Mutation | p.Arg255His(p.R255H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000375337 |
| Start | 94559017:94559017(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs571948509 |
| CDS Mutation | c.941G>A |
| AA Mutation | p.Arg314Gln(p.R314Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000375337 |
| Start | 94593579:94593579(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs376034537 |
| CDS Mutation | c.148C>T |
| AA Mutation | p.Arg50Cys(p.R50C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000375337 |
| Start | 94563407:94563407(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.760C>T |
| AA Mutation | p.His254Tyr(p.H254Y) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000375337 |
| Start | 94587417:94587417(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.223G>A |
| AA Mutation | p.Asp75Asn(p.D75N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000375337 |
| Start | 94571486:94571486(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs144416702 |
| CDS Mutation | c.543C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000375337 |
| Start | 94559018:94559018(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs376093116 |
| CDS Mutation | c.940C>T |
| AA Mutation | p.Arg314Ter(p.R314*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |