A11V (p.Ala11Val) variant of CD8B (P10966)
A11V (p.Ala11Val) in CD8B (P10966) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The available variant effect predictions contribute to a CATVariant prioritization score of 0.14 / 1. The record also includes population frequency data and structural context.
A11V (p.Ala11Val) variant details
- p.Ala11Val
- rs1202642059
- TOPMed rs1202642059
- gnomAD rs1202642059
- Variant assessed as somatic; moderate impact.
- Missense
- Variant Prioritization Score for Impact Estimate 0.136
- REVEL 0.03
- MetaLR 0.06
- MetaSVM -1.01
- CADD 13.80
- PolyPhen-2 0.13
- SIFT 0.82
- UniProt: Variant assessed as somatic; moderate impact.
- Population evidence available
- Structural context available