Primary Site >> Esophagus Cancer
Gene >> FGF8
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000344255 |
| Start | 101770442:101770442(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.589C>T |
| AA Mutation | p.Pro197Ser(p.P197S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |