Primary Site >> Esophagus Cancer
Gene >> EPHX2
| ID | 1 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000521400 |
| Start | 27541474:27541474(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1381G>A |
| AA Mutation | p.Gly461Ser(p.G461S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |