A37T (p.Ala37Thr) variant of HSD3B2 (P26439)
A37T (p.Ala37Thr) in HSD3B2 (P26439) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.23 / 1. The record also includes population frequency data and structural context.
A37T (p.Ala37Thr) variant details
- p.Ala37Thr
- ExAC rs759756499
- gnomAD rs759756499
- Missense
- Variant Prioritization Score for Impact Estimate 0.231
- REVEL 0.23
- MetaLR 0.17
- MetaSVM -0.90
- CADD 8.12
- PolyPhen-2 0.01
- SIFT 0.68
- Most common in the South Asian population (allele frequency 2.3e-05)
- Structural context available