Primary Site >> Stomach Cancer
Gene >> FBXO7
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000266087 |
| Start | 32483943:32483943(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs61730784 |
| CDS Mutation | c.464C>T |
| AA Mutation | p.Ala155Val(p.A155V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000266087 |
| Start | 32498459:32498459(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs113341800 |
| CDS Mutation | c.1498G>A |
| AA Mutation | p.Gly500Ser(p.G500S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000266087 |
| Start | 32485133:32485133(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.711G>T |
| AA Mutation | p.Gln237His(p.Q237H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000266087 |
| Start | 32491105:32491105(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs146429630 |
| CDS Mutation | c.891A>G |
| AA Mutation | p.Ile297Met(p.I297M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000266087 |
| Start | 32484021:32484021(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.542A>C |
| AA Mutation | p.His181Pro(p.H181P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000266087 |
| Start | 32498329:32498329(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs771788871 |
| CDS Mutation | c.1368T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000266087 |
| Start | 32498374:32498374(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs375919269 |
| CDS Mutation | c.1413G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |