P12T (p.Pro12Thr) variant of PPARG (P37231)
P12T (p.Pro12Thr) in PPARG (P37231) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.32 / 1. The record also includes population frequency data, published literature, and structural context.
P12T (p.Pro12Thr) variant details
- p.Pro12Thr
- gnomAD 3-12351626-C-A
- Missense
- Variant Prioritization Score for Impact Estimate 0.322
- CADD 19.00
- Most common in the South Asian population (allele frequency 9.3e-05)
- Structural context available
- Literature evidence available