F41S (p.Phe41Ser) variant of IL17F (Interleukin-17F)
F41S (p.Phe41Ser) in IL17F (Interleukin-17F) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. 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.
F41S (p.Phe41Ser) variant details
- p.Phe41Ser
- NCI-TCGA Cosmic COSV6023
- TOPMed rs1764017098
- gnomAD rs1764017098
- Variant assessed as somatic; moderate impact.
- Missense
- Variant Prioritization Score for Impact Estimate 0.113
- REVEL 0.07
- MetaLR 0.03
- MetaSVM -1.08
- CADD 8.20
- PolyPhen-2 0.19
- SIFT 0.45
- UniProt: Variant assessed as somatic; moderate impact.
- Most common in the Non-Finnish European population (allele frequency 1.5e-05)
- Structural context available