P42Q (p.Pro42Gln) variant of AKT1 (P31749)
P42Q (p.Pro42Gln) in AKT1 (P31749) is a missense change. Clinical records from EBI and UniProt describe it as uncertain significance. The record also includes structural context.
P42Q (p.Pro42Gln) variant details
- p.Pro42Gln
- TOPMed rs1892951094
- Uncertain significance
- Missense
- EBI: Variant of uncertain significance
- UniProt: Uncertain significance
- Structural context available