S14N (p.Ser14Asn) variant of PPARG (P37231)
S14N (p.Ser14Asn) in PPARG (P37231) is a missense 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.
S14N (p.Ser14Asn) variant details
- p.Ser14Asn
- rs1055170892
- gnomAD 3-12351633-G-A
- Missense
- Variant Prioritization Score for Impact Estimate 0.359
- CADD 16.40
- Population evidence available
- Structural context available
- Literature evidence available