H67Q (p.His67Gln) variant of CD8B (P10966)
H67Q (p.His67Gln) in CD8B (P10966) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.10 / 1. The record also includes population frequency data and structural context.
H67Q (p.His67Gln) variant details
- p.His67Gln
- ExAC rs752467151
- TOPMed rs752467151
- gnomAD rs752467151
- Missense
- Variant Prioritization Score for Impact Estimate 0.0985
- REVEL 0.08
- MetaLR 0.12
- MetaSVM -0.96
- CADD 0.01
- PolyPhen-2 0.03
- SIFT 0.07
- Most common in the South Asian population (allele frequency 0.00021)
- Structural context available