A71V (p.Ala71Val) variant of CD8B (P10966)
A71V (p.Ala71Val) in CD8B (P10966) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.19 / 1. The record also includes population frequency data and structural context.
A71V (p.Ala71Val) variant details
- p.Ala71Val
- ExAC rs765982501
- gnomAD rs765982501
- Missense
- Variant Prioritization Score for Impact Estimate 0.191
- REVEL 0.08
- MetaLR 0.08
- MetaSVM -1.08
- CADD 6.69
- PolyPhen-2 0.03
- SIFT 0.32
- Most common in the Latino/Admixed American population (allele frequency 6.5e-05)
- Structural context available