R17R (p.Arg17Arg) variant of HSD3B2 (P26439)
R17R (p.Arg17Arg) 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.
R17R (p.Arg17Arg) variant details
- p.Arg17Arg
- rs757957605
- gnomAD 1-119415470-G-A
- Synonymous
- Variant Prioritization Score for Impact Estimate 0.34
- CADD 9.15
- Most common in the South Asian population (allele frequency 0.00021)
- Structural context available
- Literature evidence available