D7V (p.Asp7Val) variant of PPARG (P37231)
D7V (p.Asp7Val) in PPARG (P37231) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.58 / 1. The record also includes population frequency data, published literature, and structural context.
D7V (p.Asp7Val) variant details
- p.Asp7Val
- gnomAD 3-12351612-A-T
- Missense
- Variant Prioritization Score for Impact Estimate 0.577
- CADD 22.10
- Most common in the Non-Finnish European population (allele frequency 1.8e-06)
- Structural context available
- Literature evidence available