P39H (p.Pro39His) variant of APOL1 (Apolipoprotein L1)
P39H (p.Pro39His) in APOL1 (Apolipoprotein L1) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.04 / 1. The record also includes population frequency data, published literature, and structural context.
P39H (p.Pro39His) variant details
- p.Pro39His
- gnomAD 22-36254918-C-A
- Missense
- Variant Prioritization Score for Impact Estimate 0.0406
- CADD 0.20
- SIFT 0.00
- Most common in the REMAINING population (allele frequency 1.7e-05)
- Structural context available
- Literature evidence available