Primary Site >> Pancreatic Cancer
Gene >> MCHR2
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000281806 |
| Start | 99947799:99947799(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.355G>A |
| AA Mutation | p.Ala119Thr(p.A119T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |