V7V (p.Val7Val) variant of HSD3B2 (P26439)
V7V (p.Val7Val) in HSD3B2 (P26439) is a synonymous change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.20 / 1. The record also includes population frequency data, published literature, and structural context.
V7V (p.Val7Val) variant details
- p.Val7Val
- gnomAD 1-119415440-G-A
- Synonymous
- Variant Prioritization Score for Impact Estimate 0.202
- CADD 7.44
- Most common in the Non-Finnish European population (allele frequency 1.8e-06)
- Structural context available
- Literature evidence available