F38V (p.Phe38Val) variant of PPARG (P37231)
F38V (p.Phe38Val) in PPARG (P37231) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.62 / 1. The record also includes population frequency data, published literature, and structural context.
F38V (p.Phe38Val) variant details
- p.Phe38Val
- rs1413870551
- gnomAD 3-12379829-T-G
- Missense
- Variant Prioritization Score for Impact Estimate 0.622
- CADD 23.90
- PolyPhen-2 0.45
- SIFT 0.30
- Most common in the African/African-American population (allele frequency 3e-05)
- Structural context available
- Literature evidence available