A13V (p.Ala13Val) variant of HNF4A (P41235)
A13V (p.Ala13Val) in HNF4A (P41235) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.22 / 1. The record also includes population frequency data, published literature, and structural context.
A13V (p.Ala13Val) variant details
- p.Ala13Val
- rs1051122101
- gnomAD 20-44355821-C-T
- Missense
- Variant Prioritization Score for Impact Estimate 0.217
- CADD 19.30
- Population evidence available
- Structural context available
- Literature evidence available