P37S (p.Pro37Ser) variant of LRBA (P50851)
P37S (p.Pro37Ser) in LRBA (P50851) is a missense change. Clinical records from ClinVar, EBI, and UniProt describe it as uncertain significance in the context of Combined immunodeficiency due to LRBA deficiency. The available variant effect predictions contribute to a CATVariant prioritization score of 0.58 / 1. The record also includes population frequency data.
P37S (p.Pro37Ser) variant details
- p.Pro37Ser
- rs374519451
- ClinGen CA3103968
- ClinVar RCV001313670
- ClinVar RCV004570742
- Uncertain significance
- Combined immunodeficiency due to LRBA deficiency
- Missense
- Variant Prioritization Score for Impact Estimate 0.579
- MetaLR 0.43
- MetaSVM -0.14
- CADD 23.50
- PolyPhen-2 1.00
- SIFT 0.00
- ClinVar: Uncertain significance (Combined immunodeficiency due to LRBA deficiency)
- EBI: Variant of uncertain significance
- UniProt: Uncertain significance
- Most common in the Middle Eastern population (allele frequency 0.00017)