S16G (p.Ser16Gly) variant of PPARG (P37231)
S16G (p.Ser16Gly) in PPARG (P37231) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.61 / 1. The record also includes population frequency data, published literature, and structural context.
S16G (p.Ser16Gly) variant details
- p.Ser16Gly
- gnomAD 3-12379757-A-G
- Missense
- Variant Prioritization Score for Impact Estimate 0.614
- CADD 18.60
- PolyPhen-2 0.01
- SIFT 0.11
- Most common in the Non-Finnish European population (allele frequency 9e-07)
- Structural context available
- Literature evidence available