A13T (p.Ala13Thr) variant of HNF4A (P41235)
A13T (p.Ala13Thr) in HNF4A (P41235) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.32 / 1. The record also includes population frequency data, published literature, and structural context.
A13T (p.Ala13Thr) variant details
- p.Ala13Thr
- rs2062850800
- gnomAD 20-44355820-G-A
- Missense
- Variant Prioritization Score for Impact Estimate 0.324
- CADD 22.50
- Population evidence available
- Structural context available
- Literature evidence available