Primary Site >> Esophagus Cancer
Gene >> ANXA2
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000396024 |
| Start | 60352426:60352426(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.639G>C |
| AA Mutation | p.Trp213Cys(p.W213C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |