A37G (p.Ala37Gly) variant of HSD3B2 (P26439)
A37G (p.Ala37Gly) in HSD3B2 (P26439) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.25 / 1. The record also includes population frequency data and structural context.
A37G (p.Ala37Gly) variant details
- p.Ala37Gly
- ExAC rs767793086
- TOPMed rs767793086
- gnomAD rs767793086
- Missense
- Variant Prioritization Score for Impact Estimate 0.255
- REVEL 0.33
- MetaLR 0.35
- MetaSVM -0.58
- CADD 3.90
- PolyPhen-2 0.10
- SIFT 0.44
- Most common in the Non-Finnish European population (allele frequency 2.9e-05)
- Structural context available