Y78H (p.Tyr78His) variant of PPARG (P37231)
Y78H (p.Tyr78His) in PPARG (P37231) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.63 / 1. The record also includes population frequency data and published literature.
Y78H (p.Tyr78His) variant details
- p.Tyr78His
- gnomAD 3-12379853-T-C
- Missense
- Variant Prioritization Score for Impact Estimate 0.628
- CADD 23.70
- PolyPhen-2 0.95
- SIFT 0.47
- Most common in the Non-Finnish European population (allele frequency 9e-07)
- Literature evidence available