A91V (p.Ala91Val) variant of CD8B (P10966)
A91V (p.Ala91Val) in CD8B (P10966) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.09 / 1. The record also includes population frequency data and structural context.
A91V (p.Ala91Val) variant details
- p.Ala91Val
- Ensembl rs1676376030
- Missense
- Variant Prioritization Score for Impact Estimate 0.0892
- REVEL 0.04
- MetaLR 0.09
- MetaSVM -1.02
- CADD 4.79
- PolyPhen-2 0.05
- SIFT 0.28
- Most common in the African/African-American population (allele frequency 3e-05)
- Structural context available