P9P (p.Pro9Pro) variant of PPARG (P37231)
P9P (p.Pro9Pro) in PPARG (P37231) is a synonymous change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.11 / 1. The record also includes population frequency data, published literature, and structural context.
P9P (p.Pro9Pro) variant details
- p.Pro9Pro
- rs755878073
- gnomAD 3-12379732-A-C
- Synonymous
- Variant Prioritization Score for Impact Estimate 0.106
- CADD 3.58
- Most common in the Latino/Admixed American population (allele frequency 2.2e-05)
- Structural context available
- Literature evidence available