H17R (p.His17Arg) variant of CD8B (P10966)
H17R (p.His17Arg) in CD8B (P10966) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.07 / 1. The record also includes population frequency data and structural context.
H17R (p.His17Arg) variant details
- p.His17Arg
- ESP rs368650240
- ExAC rs368650240
- TOPMed rs368650240
- gnomAD rs368650240
- Missense
- Variant Prioritization Score for Impact Estimate 0.0749
- REVEL 0.03
- MetaLR 0.04
- MetaSVM -1.06
- CADD 0.00
- PolyPhen-2 0.00
- SIFT 1.00
- Most common in the South Asian population (allele frequency 0.00021)
- Structural context available