Q66H (p.Gln66His) variant of FTO (Q9C0B1)
Q66H (p.Gln66His) in FTO (Q9C0B1) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.40 / 1. The record also includes population frequency data and structural context.
Q66H (p.Gln66His) variant details
- p.Gln66His
- gnomAD rs1414523806
- Missense
- Variant Prioritization Score for Impact Estimate 0.396
- REVEL 0.56
- CADD 14.90
- PolyPhen-2 0.89
- SIFT 0.00
- Most common in the East Asian population (allele frequency 2.5e-05)
- Structural context available