A33P (p.Ala33Pro) variant of HSD3B2 (P26439)
A33P (p.Ala33Pro) in HSD3B2 (P26439) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.55 / 1. The record also includes population frequency data, published literature, and structural context.
A33P (p.Ala33Pro) variant details
- p.Ala33Pro
- gnomAD 1-119415516-G-C
- Missense
- Variant Prioritization Score for Impact Estimate 0.552
- REVEL 0.62
- MetaLR 0.65
- MetaSVM -0.14
- CADD 17.30
- PolyPhen-2 0.70
- SIFT 0.15
- Most common in the Non-Finnish European population (allele frequency 9e-07)
- Structural context available
- Literature evidence available