F67F (p.Phe67Phe) variant of HSD3B2 (P26439)
F67F (p.Phe67Phe) in HSD3B2 (P26439) is a synonymous change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.24 / 1. The record also includes population frequency data, published literature, and structural context.
F67F (p.Phe67Phe) variant details
- p.Phe67Phe
- rs1425113240
- gnomAD 1-119419476-C-T
- Synonymous
- Variant Prioritization Score for Impact Estimate 0.244
- CADD 3.44
- Most common in the East Asian population (allele frequency 2.5e-05)
- Structural context available
- Literature evidence available