Primary Site >> Pancreatic Cancer
Gene >> STC2
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000265087 |
| Start | 173317923:173317923(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs778297660 |
| CDS Mutation | c.833G>A |
| AA Mutation | p.Gly278Asp(p.G278D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |