P39H (p.Pro39His) variant of HLA-C (P10321)
P39H (p.Pro39His) in HLA-C (P10321) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.31 / 1. The record also includes population frequency data and structural context.
P39H (p.Pro39His) variant details
- p.Pro39His
- ExAC rs281860335
- gnomAD rs281860335
- Missense
- Variant Prioritization Score for Impact Estimate 0.306
- REVEL 0.13
- CADD 26.10
- PolyPhen-2 0.98
- SIFT 0.01
- Most common in the Non-Finnish European population (allele frequency 1.1e-06)
- Structural context available