Primary Site >> Esophagus Cancer
Gene >> CRP
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000255030 |
| Start | 159713928:159713928(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.272A>G |
| AA Mutation | p.Tyr91Cys(p.Y91C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |