P86A (p.Pro86Ala) variant of CD79B (P40259)
P86A (p.Pro86Ala) in CD79B (P40259) is a missense change. Clinical records from EBI and UniProt describe it as uncertain significance. The record also includes structural context.
P86A (p.Pro86Ala) variant details
- p.Pro86Ala
- Ensembl rs1908041476
- Uncertain significance
- Missense
- EBI: Variant of uncertain significance
- UniProt: Uncertain significance
- Structural context available