Primary Site >> Pancreatic Cancer
Gene >> PAX7
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000420770 |
| Start | 18691844:18691844(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.677C>T |
| AA Mutation | p.Ala226Val(p.A226V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |