Q87R (p.Gln87Arg) variant of CD8B (P10966)
Q87R (p.Gln87Arg) 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 0.08 / 1. The record also includes population frequency data and structural context.
Q87R (p.Gln87Arg) variant details
- p.Gln87Arg
- rs1446544258
- TOPMed rs1446544258
- gnomAD rs1446544258
- Variant assessed as somatic; moderate impact.
- Missense
- Variant Prioritization Score for Impact Estimate 0.0826
- REVEL 0.03
- MetaLR 0.15
- MetaSVM -0.97
- CADD 1.75
- PolyPhen-2 0.17
- SIFT 0.13
- UniProt: Variant assessed as somatic; moderate impact.
- Most common in the African/African-American population (allele frequency 2.4e-05)
- Structural context available