A13A (p.Ala13Ala) variant of HNF4A (P41235)
A13A (p.Ala13Ala) in HNF4A (P41235) is a synonymous change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.29 / 1. The record also includes population frequency data, published literature, and structural context.
A13A (p.Ala13Ala) variant details
- p.Ala13Ala
- rs772889022
- gnomAD 20-44355834-T-C
- Synonymous
- Variant Prioritization Score for Impact Estimate 0.294
- CADD 14.70
- Most common in the Latino/Admixed American population (allele frequency 2.2e-05)
- Structural context available
- Literature evidence available