V52G (p.Val52Gly) variant of HLA-B (P01889)
V52G (p.Val52Gly) in HLA-B (P01889) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.40 / 1. The record also includes population frequency data and structural context.
V52G (p.Val52Gly) variant details
- p.Val52Gly
- gnomAD rs151341109
- Missense
- Variant Prioritization Score for Impact Estimate 0.401
- REVEL 0.33
- CADD 28.00
- PolyPhen-2 1.00
- SIFT 0.00
- Most common in the Non-Finnish European population (allele frequency 2.9e-05)
- Structural context available