Primary Site >> Pancreatic Cancer
Gene >> MIA
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000263369 |
| Start | 40775546:40775546(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.4G>A |
| AA Mutation | p.Ala2Thr(p.A2T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |