A37A (p.Ala37Ala) variant of HSD3B2 (P26439)
A37A (p.Ala37Ala) in HSD3B2 (P26439) is a synonymous change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.34 / 1. The record also includes population frequency data, published literature, and structural context.
A37A (p.Ala37Ala) variant details
- p.Ala37Ala
- rs1651679921
- gnomAD 1-119415530-C-T
- Synonymous
- Variant Prioritization Score for Impact Estimate 0.344
- CADD 5.19
- Most common in the Non-Finnish European population (allele frequency 1.5e-05)
- Structural context available
- Literature evidence available