F38F (p.Phe38Phe) variant of PPARG (P37231)
F38F (p.Phe38Phe) in PPARG (P37231) is a synonymous change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.56 / 1. The record also includes population frequency data, published literature, and structural context.
F38F (p.Phe38Phe) variant details
- p.Phe38Phe
- gnomAD 3-12379831-C-T
- Synonymous
- Variant Prioritization Score for Impact Estimate 0.559
- CADD 12.50
- Most common in the East Asian population (allele frequency 7.6e-05)
- Structural context available
- Literature evidence available