S16T (p.Ser16Thr) variant of PPARG (P37231)
S16T (p.Ser16Thr) in PPARG (P37231) is a protein-truncating change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.77 / 1. The record also includes population frequency data, published literature, and structural context.
S16T (p.Ser16Thr) variant details
- p.Ser16Thr
- gnomAD 3-12351635-GATTCC
- Frameshift
- Variant Prioritization Score for Impact Estimate 0.765
- CADD 24.10
- Most common in the Non-Finnish European population (allele frequency 9e-07)
- Structural context available
- Literature evidence available