T26N (p.Thr26Asn) variant of LRBA (P50851)
T26N (p.Thr26Asn) in LRBA (P50851) is a missense change. Clinical records from ClinVar and UniProt describe it as uncertain significance in the context of Combined immunodeficiency due to LRBA deficiency.
T26N (p.Thr26Asn) variant details
- p.Thr26Asn
- TOPMed rs1745221827
- Uncertain significance
- Combined immunodeficiency due to LRBA deficiency
- Missense
- ClinVar: Uncertain significance (Combined immunodeficiency due to LRBA deficiency)
- UniProt: Uncertain significance