M82R (p.Met82Arg) variant of CD79B (P40259)
M82R (p.Met82Arg) in CD79B (P40259) is a missense change. Clinical records from ClinVar, EBI, and UniProt describe it as uncertain significance in the context of Agammaglobulinemia 6, autosomal recessive. The record also includes structural context.
M82R (p.Met82Arg) variant details
- p.Met82Arg
- rs2509269003
- ClinGen CA400604846
- ClinVar RCV003630555
- Uncertain significance
- Agammaglobulinemia 6, autosomal recessive
- Missense
- ClinVar: Uncertain significance (Agammaglobulinemia 6, autosomal recessive)
- EBI: Variant of uncertain significance
- UniProt: Uncertain significance
- Structural context available