A68G (p.Ala68Gly) variant of FTO (Q9C0B1)
A68G (p.Ala68Gly) in FTO (Q9C0B1) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.62 / 1. The record also includes population frequency data and structural context.
A68G (p.Ala68Gly) variant details
- p.Ala68Gly
- gnomAD rs555319581
- Missense
- Variant Prioritization Score for Impact Estimate 0.619
- REVEL 0.51
- CADD 23.40
- PolyPhen-2 1.00
- SIFT 0.17
- Most common in the South Asian population (allele frequency 0.00021)
- Structural context available