R39H (p.Arg39His) variant of XPA (P23025)
R39H (p.Arg39His) in XPA (P23025) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.40 / 1. The record also includes population frequency data and structural context.
R39H (p.Arg39His) variant details
- p.Arg39His
- gnomAD rs1328849329
- Missense
- Variant Prioritization Score for Impact Estimate 0.398
- REVEL 0.27
- CADD 25.00
- PolyPhen-2 0.01
- SIFT 0.00
- Most common in the Non-Finnish European population (allele frequency 1.5e-05)
- Structural context available