S56N (p.Ser56Asn) variant of FTO (Q9C0B1)
S56N (p.Ser56Asn) in FTO (Q9C0B1) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.24 / 1. The record also includes population frequency data, published literature, and structural context.
S56N (p.Ser56Asn) variant details
- p.Ser56Asn
- gnomAD 16-53825907-G-A
- Missense
- Variant Prioritization Score for Impact Estimate 0.238
- REVEL 0.19
- CADD 18.70
- PolyPhen-2 0.31
- SIFT 0.06
- Most common in the South Asian population (allele frequency 1.2e-05)
- Structural context available
- Literature evidence available