H17N (p.His17Asn) variant of CD8A (P01732)
H17N (p.His17Asn) in CD8A (P01732) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.19 / 1. The record also includes population frequency data.
H17N (p.His17Asn) variant details
- p.His17Asn
- TOPMed rs868233441
- gnomAD rs868233441
- Missense
- Variant Prioritization Score for Impact Estimate 0.19
- REVEL 0.17
- MetaLR 0.33
- MetaSVM -0.80
- CADD 10.10
- PolyPhen-2 0.02
- SIFT 0.52
- Most common in the Non-Finnish European population (allele frequency 1.8e-06)