A53D (p.Ala53Asp) variant of PLCG2 (P16885)
A53D (p.Ala53Asp) in PLCG2 (P16885) is a missense change. The record also includes experimental measurements and structural context.
A53D (p.Ala53Asp) variant details
- p.Ala53Asp
- TOPMed rs1253716514
- gnomAD rs1253716514
- Missense
- Structural context available
- PLCG2 SH3 domain domainome 1.0: score -0.177