R107Q (p.Arg107Gln) variant of CD8A (P01732)
R107Q (p.Arg107Gln) in CD8A (P01732) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.11 / 1. The record also includes population frequency data.
R107Q (p.Arg107Gln) variant details
- p.Arg107Gln
- ExAC rs780835924
- TOPMed rs780835924
- gnomAD rs780835924
- Missense
- Variant Prioritization Score for Impact Estimate 0.114
- REVEL 0.06
- MetaLR 0.12
- MetaSVM -1.05
- CADD 9.06
- PolyPhen-2 0.00
- SIFT 0.25
- Most common in the East Asian population (allele frequency 2.5e-05)