F28F (p.Phe28Phe) variant of HNF4A (P41235)
F28F (p.Phe28Phe) in HNF4A (P41235) is a synonymous change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.33 / 1. The record also includes population frequency data, published literature, and structural context.
F28F (p.Phe28Phe) variant details
- p.Phe28Phe
- rs549449127
- gnomAD 20-44390663-C-T
- Synonymous
- Variant Prioritization Score for Impact Estimate 0.329
- CADD 14.20
- Most common in the South Asian population (allele frequency 1.6e-05)
- Structural context available
- Literature evidence available