R38Q (p.Arg38Gln) variant of HLA-C (P10321)
R38Q (p.Arg38Gln) in HLA-C (P10321) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.32 / 1. The record also includes population frequency data and structural context.
R38Q (p.Arg38Gln) variant details
- p.Arg38Gln
- ExAC rs72558134
- gnomAD rs72558134
- Missense
- Variant Prioritization Score for Impact Estimate 0.323
- REVEL 0.20
- CADD 22.80
- PolyPhen-2 0.01
- SIFT 0.04
- Most common in the Non-Finnish European population (allele frequency 2.2e-05)
- Structural context available