Primary Site >> Esophagus Cancer
Gene >> NDRG2
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000298687 |
| Start | 21019137:21019137(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs747046310 |
| CDS Mutation | c.740G>A |
| AA Mutation | p.Arg247His(p.R247H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |