A13V (p.Ala13Val) variant of CD8A (P01732)
A13V (p.Ala13Val) in CD8A (P01732) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.30 / 1. The record also includes population frequency data.
A13V (p.Ala13Val) variant details
- p.Ala13Val
- ExAC rs766551828
- gnomAD rs766551828
- Missense
- Variant Prioritization Score for Impact Estimate 0.296
- REVEL 0.20
- MetaLR 0.25
- MetaSVM -0.97
- CADD 14.90
- PolyPhen-2 0.00
- SIFT 0.41
- Most common in the HGDP:BURUSHO population (allele frequency 0.042)