D9G (p.Asp9Gly) variant of HNF4A (P41235)
D9G (p.Asp9Gly) in HNF4A (P41235) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.20 / 1. The record also includes population frequency data, published literature, and structural context.
D9G (p.Asp9Gly) variant details
- p.Asp9Gly
- rs1198174462
- gnomAD 20-44390647-A-G
- Missense
- Variant Prioritization Score for Impact Estimate 0.2
- CADD 16.80
- Most common in the Non-Finnish European population (allele frequency 1.3e-05)
- Structural context available
- Literature evidence available