R32S (p.Arg32Ser) variant of TNFRSF13B (O14836)
R32S (p.Arg32Ser) in TNFRSF13B (O14836) is a missense change. Clinical records from ClinVar, EBI, and UniProt describe it as uncertain significance in the context of Immunodeficiency, common variable, 2.
R32S (p.Arg32Ser) variant details
- p.Arg32Ser
- rs2508218579
- ClinGen CA398520497
- ClinVar RCV002885875
- Uncertain significance
- Immunodeficiency, common variable, 2
- Missense
- ClinVar: Uncertain significance (Immunodeficiency, common variable, 2)
- EBI: Variant of uncertain significance
- UniProt: Uncertain significance