R38G (p.Arg38Gly) variant of HLA-B (P01889)
R38G (p.Arg38Gly) in HLA-B (P01889) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.35 / 1. The record also includes population frequency data and structural context.
R38G (p.Arg38Gly) variant details
- p.Arg38Gly
- gnomAD rs1338962119
- Missense
- Variant Prioritization Score for Impact Estimate 0.347
- REVEL 0.20
- CADD 26.40
- PolyPhen-2 1.00
- SIFT 0.00
- Most common in the Non-Finnish European population (allele frequency 1e-05)
- Structural context available