S4W (p.Ser4Trp) variant of HNF4A (P41235)
S4W (p.Ser4Trp) in HNF4A (P41235) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.70 / 1. The record also includes population frequency data, published literature, and structural context.
S4W (p.Ser4Trp) variant details
- p.Ser4Trp
- rs780566668
- gnomAD 20-44390644-C-G
- Missense
- Variant Prioritization Score for Impact Estimate 0.696
- CADD 21.50
- Most common in the Latino/Admixed American population (allele frequency 2.9e-05)
- Structural context available
- Literature evidence available