G37V (p.Gly37Val) variant of HNF4A (P41235)
G37V (p.Gly37Val) in HNF4A (P41235) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.32 / 1. The record also includes population frequency data, published literature, and structural context.
G37V (p.Gly37Val) variant details
- p.Gly37Val
- gnomAD 20-44390653-G-T
- Missense
- Variant Prioritization Score for Impact Estimate 0.315
- CADD 18.00
- Population evidence available
- Structural context available
- Literature evidence available