Primary Site >> Pancreatic Cancer
Gene >> ITGAL
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000356798 |
| Start | 30494322:30494322(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs749508499 |
| CDS Mutation | c.1324G>A |
| AA Mutation | p.Gly442Arg(p.G442R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |