A96V (p.Ala96Val) variant of CD8B (P10966)
A96V (p.Ala96Val) in CD8B (P10966) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.12 / 1. The record also includes population frequency data and structural context.
A96V (p.Ala96Val) variant details
- p.Ala96Val
- TOPMed rs1310724979
- gnomAD rs1310724979
- Missense
- Variant Prioritization Score for Impact Estimate 0.118
- REVEL 0.11
- MetaLR 0.15
- MetaSVM -0.93
- CADD 0.05
- SIFT 0.25
- Most common in the African/African-American population (allele frequency 4.8e-05)
- Structural context available