G27A (p.Gly27Ala) variant of CD79A (P11912)
G27A (p.Gly27Ala) in CD79A (P11912) is a missense change. Clinical records from EBI and UniProt describe it as uncertain significance. The record also includes structural context.
G27A (p.Gly27Ala) variant details
- p.Gly27Ala
- TOPMed rs2074204427
- Uncertain significance
- Missense
- EBI: Variant of uncertain significance
- UniProt: Uncertain significance
- Structural context available