A56T (p.Ala56Thr) variant of APOL1 (Apolipoprotein L1)
A56T (p.Ala56Thr) in APOL1 (Apolipoprotein L1) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.08 / 1. The record also includes population frequency data and structural context.
A56T (p.Ala56Thr) variant details
- p.Ala56Thr
- gnomAD rs1418883562
- Missense
- Variant Prioritization Score for Impact Estimate 0.081
- REVEL 0.10
- CADD 0.04
- PolyPhen-2 0.00
- SIFT 0.08
- Most common in the South Asian population (allele frequency 2.3e-05)
- Structural context available