Primary Site >> Esophagus Cancer
Gene >> FCER2
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000346664 |
| Start | 7696906:7696906(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs755933015 |
| CDS Mutation | c.388G>A |
| AA Mutation | p.Glu130Lys(p.E130K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |