Primary Site >> Esophagus Cancer
Gene >> PGF
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000405431 |
| Start | 74946753:74946753(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.588C>A |
| AA Mutation | p.Asn196Lys(p.N196K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |