S4A (p.Ser4Ala) variant of HNF4A (P41235)
S4A (p.Ser4Ala) in HNF4A (P41235) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.34 / 1. The record also includes population frequency data, published literature, and structural context.
S4A (p.Ser4Ala) variant details
- p.Ser4Ala
- gnomAD 20-44390643-T-G
- Missense
- Variant Prioritization Score for Impact Estimate 0.336
- CADD 19.80
- Most common in the Non-Finnish European population (allele frequency 3.2e-06)
- Structural context available
- Literature evidence available