W3R (p.Trp3Arg) variant of HSD3B2 (P26439)
W3R (p.Trp3Arg) in HSD3B2 (P26439) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.40 / 1. The record also includes population frequency data, published literature, and structural context.
W3R (p.Trp3Arg) variant details
- p.Trp3Arg
- gnomAD 1-119415426-T-A
- Missense
- Variant Prioritization Score for Impact Estimate 0.401
- REVEL 0.35
- MetaLR 0.21
- MetaSVM -0.68
- CADD 22.80
- PolyPhen-2 0.79
- SIFT 0.35
- Most common in the Non-Finnish European population (allele frequency 9e-07)
- Structural context available
- Literature evidence available