Primary Site >> Esophagus Cancer
Gene >> AMH
| ID | 1 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000221496 |
| Start | 2250425:2250425(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs779588404 |
| CDS Mutation | c.501C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |