Y15N (p.Tyr15Asn) variant of HNF4A (P41235)
Y15N (p.Tyr15Asn) in HNF4A (P41235) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.61 / 1. The record also includes population frequency data, published literature, and structural context.
Y15N (p.Tyr15Asn) variant details
- p.Tyr15Asn
- gnomAD 20-44355850-T-A
- Missense
- Variant Prioritization Score for Impact Estimate 0.609
- CADD 22.80
- Most common in the Non-Finnish European population (allele frequency 1.8e-06)
- Structural context available
- Literature evidence available