S46P (p.Ser46Pro) variant of PPARG (P37231)
S46P (p.Ser46Pro) in PPARG (P37231) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.49 / 1. The record also includes population frequency data and published literature.
S46P (p.Ser46Pro) variant details
- p.Ser46Pro
- gnomAD 3-12379832-T-C
- Missense
- Variant Prioritization Score for Impact Estimate 0.494
- CADD 22.60
- PolyPhen-2 0.01
- SIFT 0.11
- Most common in the Non-Finnish European population (allele frequency 9e-07)
- Literature evidence available