H56N (p.His56Asn) variant of PPARG (P37231)
H56N (p.His56Asn) in PPARG (P37231) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.71 / 1. The record also includes population frequency data and published literature.
H56N (p.His56Asn) variant details
- p.His56Asn
- gnomAD 3-12379793-C-A
- Missense
- Variant Prioritization Score for Impact Estimate 0.709
- CADD 20.40
- PolyPhen-2 0.02
- SIFT 0.20
- Population evidence available
- Literature evidence available