F39F (p.Phe39Phe) variant of PTH1R (Q03431)
F39F (p.Phe39Phe) in PTH1R (Q03431) is a synonymous change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.29 / 1. The record also includes population frequency data, published literature, and structural context.
F39F (p.Phe39Phe) variant details
- p.Phe39Phe
- rs552828104
- gnomAD 3-46893948-C-T
- Synonymous
- Variant Prioritization Score for Impact Estimate 0.293
- CADD 13.80
- Most common in the 1KG:KHV population (allele frequency 0.005)
- Structural context available
- Literature evidence available