R98Q (p.Arg98Gln) variant of CD8B (P10966)
R98Q (p.Arg98Gln) in CD8B (P10966) is a missense change. Clinical records from ClinVar, EBI, and UniProt describe it as uncertain significance in the context of not specified. The available variant effect predictions contribute to a CATVariant prioritization score of 0.13 / 1. The record also includes population frequency data and structural context.
R98Q (p.Arg98Gln) variant details
- p.Arg98Gln
- rs768017195
- ClinGen CA1751562
- ClinVar RCV004302590
- ExAC rs768017195
- Uncertain significance
- not specified
- Missense
- Variant Prioritization Score for Impact Estimate 0.129
- REVEL 0.13
- MetaLR 0.11
- MetaSVM -0.87
- CADD 2.15
- PolyPhen-2 0.05
- SIFT 0.25
- ClinVar: Uncertain significance (not specified)
- EBI: Variant of uncertain significance
- UniProt: Uncertain significance
- Most common in the African/African-American population (allele frequency 0.00012)
- Structural context available