Primary Site >> Esophagus Cancer
Gene >> FCGR3A
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367967 |
| Start | 161548573:161548573(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.167A>C |
| AA Mutation | p.Asn56Thr(p.N56T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |