T30N (p.Thr30Asn) variant of PPARG (P37231)
T30N (p.Thr30Asn) in PPARG (P37231) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.41 / 1. The record also includes population frequency data, published literature, and structural context.
T30N (p.Thr30Asn) variant details
- p.Thr30Asn
- rs780983036
- gnomAD 3-12379710-C-A
- Missense
- Variant Prioritization Score for Impact Estimate 0.41
- CADD 12.70
- Most common in the Non-Finnish European population (allele frequency 9e-07)
- Structural context available
- Literature evidence available