Primary Site >> Pancreatic Cancer
Gene >> FGR
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000374003 |
| Start | 27613042:27613042(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1462T>C |
| AA Mutation | p.Tyr488His(p.Y488H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |