Y78S (p.Tyr78Ser) variant of PPARG (P37231)
Y78S (p.Tyr78Ser) 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 and published literature.
Y78S (p.Tyr78Ser) variant details
- p.Tyr78Ser
- gnomAD 3-12381355-A-C
- Missense
- Variant Prioritization Score for Impact Estimate 0.596
- CADD 22.20
- PolyPhen-2 0.17
- SIFT 0.58
- Most common in the Non-Finnish European population (allele frequency 9e-07)
- Literature evidence available