Primary Site >> Pancreatic Cancer
Gene >> SIM1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000262901 |
| Start | 100449401:100449401(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.505G>A |
| AA Mutation | p.Ala169Thr(p.A169T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |