G37R (p.Gly37Arg) variant of HNF4A (P41235)
G37R (p.Gly37Arg) in HNF4A (P41235) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.53 / 1. The record also includes population frequency data, published literature, and structural context.
G37R (p.Gly37Arg) variant details
- p.Gly37Arg
- rs769394388
- gnomAD 20-44355829-G-A
- Missense
- Variant Prioritization Score for Impact Estimate 0.527
- CADD 22.40
- Most common in the Finnish in Finland (FIN) population (allele frequency 1.9e-05)
- Structural context available
- Literature evidence available