S16S (p.Ser16Ser) variant of PPARG (P37231)
S16S (p.Ser16Ser) in PPARG (P37231) is a synonymous change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.36 / 1. The record also includes population frequency data, published literature, and structural context.
S16S (p.Ser16Ser) variant details
- p.Ser16Ser
- rs1040659276
- gnomAD 3-12351640-C-T
- Synonymous
- Variant Prioritization Score for Impact Estimate 0.359
- CADD 10.50
- Most common in the Latino/Admixed American population (allele frequency 6.7e-05)
- Structural context available
- Literature evidence available