G37G (p.Gly37Gly) variant of HNF4A (P41235)
G37G (p.Gly37Gly) in HNF4A (P41235) is a synonymous change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.39 / 1. The record also includes population frequency data, published literature, and structural context.
G37G (p.Gly37Gly) variant details
- p.Gly37Gly
- rs889744956
- gnomAD 20-44355831-G-T
- Synonymous
- Variant Prioritization Score for Impact Estimate 0.394
- CADD 11.60
- Most common in the African/African-American population (allele frequency 4.8e-05)
- Structural context available
- Literature evidence available