G9G (p.Gly9Gly) variant of HSD3B2 (P26439)
G9G (p.Gly9Gly) in HSD3B2 (P26439) is a synonymous change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.36 / 1. The record also includes population frequency data, published literature, and structural context.
G9G (p.Gly9Gly) variant details
- p.Gly9Gly
- gnomAD 1-119415446-A-C
- Synonymous
- Variant Prioritization Score for Impact Estimate 0.356
- CADD 8.42
- Most common in the Non-Finnish European population (allele frequency 9e-07)
- Structural context available
- Literature evidence available