P66P (p.Pro66Pro) variant of HSD3B2 (P26439)
P66P (p.Pro66Pro) in HSD3B2 (P26439) is a synonymous change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.11 / 1. The record also includes population frequency data, published literature, and structural context.
P66P (p.Pro66Pro) variant details
- p.Pro66Pro
- gnomAD 1-119419473-A-T
- Synonymous
- Variant Prioritization Score for Impact Estimate 0.112
- CADD 4.27
- Most common in the Non-Finnish European population (allele frequency 1.8e-06)
- Structural context available
- Literature evidence available