Primary Site >> Pancreatic Cancer
Gene >> AGR2
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000419304 |
| Start | 16794951:16794951(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.463G>A |
| AA Mutation | p.Ala155Thr(p.A155T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |