L59W (p.Leu59Trp) variant of HNF4A (P41235)
L59W (p.Leu59Trp) 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.
L59W (p.Leu59Trp) variant details
- p.Leu59Trp
- rs752726625
- gnomAD 20-44402582-T-G
- Missense
- Variant Prioritization Score for Impact Estimate 0.0939
- CADD 2.59
- Most common in the Latino/Admixed American population (allele frequency 6.5e-05)
- Structural context available
- Literature evidence available