A17A (p.Ala17Ala) variant of HNF4A (P41235)
A17A (p.Ala17Ala) in HNF4A (P41235) is a synonymous change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.11 / 1. The record also includes population frequency data, published literature, and structural context.
A17A (p.Ala17Ala) variant details
- p.Ala17Ala
- gnomAD 20-44401423-T-G
- Synonymous
- Variant Prioritization Score for Impact Estimate 0.107
- CADD 3.67
- Most common in the Non-Finnish European population (allele frequency 9e-07)
- Structural context available
- Literature evidence available