A27V (p.Ala27Val) variant of CD8B (P10966)
A27V (p.Ala27Val) in CD8B (P10966) 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 and structural context.
A27V (p.Ala27Val) variant details
- p.Ala27Val
- gnomAD rs1391620375
- Missense
- Variant Prioritization Score for Impact Estimate 0.109
- REVEL 0.10
- MetaLR 0.13
- MetaSVM -0.98
- CADD 0.00
- PolyPhen-2 0.04
- SIFT 0.26
- Most common in the Finnish in Finland (FIN) population (allele frequency 9.5e-05)
- Structural context available