Primary Site >> Pancreatic Cancer
Gene >> SCGN
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000377961 |
| Start | 25670030:25670030(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.425A>T |
| AA Mutation | p.Lys142Ile(p.K142I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |