R67G (p.Arg67Gly) variant of IL17F (Interleukin-17F)
R67G (p.Arg67Gly) in IL17F (Interleukin-17F) is a missense change. Clinical records from EBI and UniProt describe it as uncertain significance. The available variant effect predictions contribute to a CATVariant prioritization score of 0.13 / 1. The record also includes population frequency data and structural context.
R67G (p.Arg67Gly) variant details
- p.Arg67Gly
- ExAC rs754476266
- TOPMed rs754476266
- gnomAD rs754476266
- Uncertain significance
- Missense
- Variant Prioritization Score for Impact Estimate 0.129
- REVEL 0.06
- MetaLR 0.02
- MetaSVM -0.96
- CADD 2.56
- SIFT 1.00
- EBI: Variant of uncertain significance
- UniProt: Uncertain significance
- Most common in the Non-Finnish European population (allele frequency 1.5e-05)
- Structural context available