Primary Site >> Esophagus Cancer
Gene >> FGFR1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000447712 |
| Start | 38429685:38429685(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.355T>G |
| AA Mutation | p.Ser119Ala(p.S119A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |