Y13N (p.Tyr13Asn) variant of PLCG2 (P16885)
Y13N (p.Tyr13Asn) in PLCG2 (P16885) is a missense change. The record also includes experimental measurements and structural context.
Y13N (p.Tyr13Asn) variant details
- p.Tyr13Asn
- TOPMed rs1910954092
- Missense
- Structural context available
- PLCG2 SH3 domain domainome 1.0: score -0.0997