R66M (p.Arg66Met) variant of HNF4A (P41235)
R66M (p.Arg66Met) in HNF4A (P41235) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.10 / 1. The record also includes population frequency data, published literature, and structural context.
R66M (p.Arg66Met) variant details
- p.Arg66Met
- gnomAD 20-44402585-G-T
- Missense
- Variant Prioritization Score for Impact Estimate 0.0957
- CADD 2.42
- Population evidence available
- Structural context available
- Literature evidence available