F17I (p.Phe17Ile) variant of PPARG (P37231)
F17I (p.Phe17Ile) in PPARG (P37231) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.60 / 1. The record also includes population frequency data, published literature, and structural context.
F17I (p.Phe17Ile) variant details
- p.Phe17Ile
- gnomAD 3-12379748-T-A
- Missense
- Variant Prioritization Score for Impact Estimate 0.604
- CADD 24.30
- PolyPhen-2 0.17
- SIFT 0.03
- Most common in the Non-Finnish European population (allele frequency 8.1e-06)
- Structural context available
- Literature evidence available