Primary Site >> Esophagus Cancer
Gene >> VNN2
| ID | 1 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000326499 |
| Start | 132751247:132751247(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1098C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |