Primary Site >> Pancreatic Cancer
Gene >> ELAVL3
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000359227 |
| Start | 11458145:11458145(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.629C>T |
| AA Mutation | p.Thr210Met(p.T210M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |