Primary Site >> Biliary tract Cancer
Gene >> CR2
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367058 |
| Start | 207469920:207469920(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1043C>A |
| AA Mutation | p.Ala348Glu(p.A348E) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |