Primary Site >> Esophagus Cancer
Gene >> VDR
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000229022 |
| Start | 47844826:47844826(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1204C>G |
| AA Mutation | p.Arg402Gly(p.R402G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |