D7G (p.Asp7Gly) variant of PPARG (P37231)
D7G (p.Asp7Gly) 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.
D7G (p.Asp7Gly) variant details
- p.Asp7Gly
- rs1447983492
- gnomAD 3-12351612-A-G
- Missense
- Variant Prioritization Score for Impact Estimate 0.58
- CADD 22.50
- Most common in the Non-Finnish European population (allele frequency 1.5e-05)
- Structural context available
- Literature evidence available