R66G (p.Arg66Gly) variant of HNF4A (P41235)
R66G (p.Arg66Gly) in HNF4A (P41235) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.09 / 1. The record also includes population frequency data, published literature, and structural context.
R66G (p.Arg66Gly) variant details
- p.Arg66Gly
- rs542742235
- gnomAD 20-44402584-A-G
- Missense
- Variant Prioritization Score for Impact Estimate 0.0944
- CADD 1.94
- Most common in the 1KG:MSL population (allele frequency 0.0063)
- Structural context available
- Literature evidence available