R38Q (p.Arg38Gln) variant of HLA-B (P01889)
R38Q (p.Arg38Gln) in HLA-B (P01889) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.36 / 1. The record also includes population frequency data and structural context.
R38Q (p.Arg38Gln) variant details
- p.Arg38Gln
- cosmic curated COSV10443
- Ensembl rs79051037
- Missense
- Variant Prioritization Score for Impact Estimate 0.36
- REVEL 0.20
- CADD 28.60
- PolyPhen-2 1.00
- SIFT 0.03
- Population evidence available
- Structural context available