Primary Site >> Pancreatic Cancer
Gene >> WNT7B
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000339464 |
| Start | 45931363:45931363(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.305G>A |
| AA Mutation | p.Arg102His(p.R102H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |