H38R (p.His38Arg) variant of IL17F (Interleukin-17F)
H38R (p.His38Arg) in IL17F (Interleukin-17F) 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 and structural context.
H38R (p.His38Arg) variant details
- p.His38Arg
- gnomAD rs1248079294
- Missense
- Variant Prioritization Score for Impact Estimate 0.112
- REVEL 0.12
- MetaLR 0.02
- MetaSVM -1.07
- CADD 0.01
- PolyPhen-2 0.00
- SIFT 0.49
- Most common in the Finnish in Finland (FIN) population (allele frequency 1.9e-05)
- Structural context available