Primary Site >> Pancreatic Cancer
Gene >> HSPB8
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000281938 |
| Start | 119193848:119193848(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs760718525 |
| CDS Mutation | c.581C>T |
| AA Mutation | p.Thr194Ile(p.T194I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |