L59R (p.Leu59Arg) variant of HNF4A (P41235)
L59R (p.Leu59Arg) in HNF4A (P41235) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.18 / 1. The record also includes population frequency data, published literature, and structural context.
L59R (p.Leu59Arg) variant details
- p.Leu59Arg
- rs1402632426
- gnomAD 20-44402573-T-G
- Missense
- Variant Prioritization Score for Impact Estimate 0.185
- CADD 2.44
- Most common in the African/African-American population (allele frequency 2.4e-05)
- Structural context available
- Literature evidence available