Primary Site >> Biliary tract Cancer
Gene >> TNFRSF10D
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000312584 |
| Start | 23145898:23145898(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.506T>C |
| AA Mutation | p.Val169Ala(p.V169A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |