P38A (p.Pro38Ala) variant of PLCG2 (P16885)
P38A (p.Pro38Ala) in PLCG2 (P16885) is a missense change. The record also includes experimental measurements and structural context.
P38A (p.Pro38Ala) variant details
- p.Pro38Ala
- TOPMed rs1910958396
- Missense
- Structural context available
- PLCG2 SH3 domain domainome 1.0: score -0.803