S16F (p.Ser16Phe) variant of PPARG (P37231)
S16F (p.Ser16Phe) in PPARG (P37231) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.41 / 1. The record also includes population frequency data, published literature, and structural context.
S16F (p.Ser16Phe) variant details
- p.Ser16Phe
- rs560683642
- gnomAD 3-12351639-C-T
- Missense
- Variant Prioritization Score for Impact Estimate 0.412
- CADD 18.30
- Most common in the South Asian population (allele frequency 1.2e-05)
- Structural context available
- Literature evidence available