Primary Site >> Esophagus Cancer
Gene >> NGFR
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000172229 |
| Start | 49506401:49506401(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.311A>T |
| AA Mutation | p.Asp104Val(p.D104V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |