C13G (p.Cys13Gly) variant of APOL1 (Apolipoprotein L1)
C13G (p.Cys13Gly) in APOL1 (Apolipoprotein L1) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.18 / 1. The record also includes population frequency data, published literature, and structural context.
C13G (p.Cys13Gly) variant details
- p.Cys13Gly
- gnomAD 22-36254929-T-G
- Missense
- Variant Prioritization Score for Impact Estimate 0.183
- CADD 5.94
- SIFT 0.00
- Most common in the Non-Finnish European population (allele frequency 9e-07)
- Structural context available
- Literature evidence available