Primary Site >> Pancreatic Cancer
Gene >> NEFM
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000221166 |
| Start | 24914667:24914667(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.874T>C |
| AA Mutation | p.Phe292Leu(p.F292L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |