W27G (p.Trp27Gly) variant of FTO (Q9C0B1)
W27G (p.Trp27Gly) in FTO (Q9C0B1) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.11 / 1. The record also includes population frequency data, published literature, and structural context.
W27G (p.Trp27Gly) variant details
- p.Trp27Gly
- rs564070241
- gnomAD 16-53711449-T-G
- Missense
- Variant Prioritization Score for Impact Estimate 0.111
- CADD 7.04
- SIFT 0.33
- Most common in the 1KG:MSL population (allele frequency 0.0063)
- Structural context available
- Literature evidence available