IL17RC p.Val342=
c.1026C>T · VCV3689163
Likely benign
Single submitter
Classification
Likely benign
ClinVar
Review
Single submitter ★☆☆☆
ClinVar · 1 submitter
gnomAD v4.1
Absent
absent from gnomAD v4.1
Conditions
1
candidiasis, familial, 9
Computational evidence
| Protein change | ||
| Missense predictors do not apply to this variant type; conservation carries the signal. | ||
| Splicing | ||
| SpliceAI | — | not assessed · no allele here is in the release |
|---|---|---|
| Constraint at this position | ||
| Conservation | phyloP -1.6 | GERP -3.1 |
| Overall | ||
| CADD | 0.543 | PHRED · no single calibrated threshold — expert panels disagree |
Population frequency
gnomAD v4.1 · exomes + genomes
Absent from gnomAD v4.1. Not observed in any sequenced alleles — a rarity signal (ACMG PM2-supporting), not evidence of pathogenicity on its own.
Variant & gene context
- Gene
- IL17RC
- Protein
- p.Val342=
- Coding
- c.1026C>T
- MANE Select
- NM_153460
- Type
- single nucleotide variant
- Location
- chr3:9928453 (GRCh38)
- Gene constraint
- LOEUF 0.777 · pLI <0.01 (gnomAD)
- Structure
- AlphaFold pLDDT 74.19 · 5 PDB
- Residue 342
- a disulfide bond; a β-strand
Disease context
candidiasis, familial, 9 — disease report on Sugi Atlas → Associated genes, phenotypes, clinical trials & treatmentsFor Chronic mucocutaneous candidiasis (Orphanet):
- Inheritance
- Autosomal dominant, Autosomal recessive
- Onset
- Childhood, Infancy
Similar variants
- IL17RC c.105+146G>A Uncertain significance ★★ ⚠ same condition
- IL17RC c.105+25G>A Uncertain significance ★★ ⚠ same condition
- IL17RC c.105+33G>T Uncertain significance ★★ ⚠ same condition
- IL17RC c.106-144G>A Uncertain significance ★★ ⚠ same condition
- IL17RC p.Ala166Val Uncertain significance ★★ ⚠ same condition
- IL17RC p.Ala30Ser Uncertain significance ★★ ⚠ same condition
- IL17RC p.Ala326Thr Uncertain significance ★★ ⚠ same condition
- IL17RC p.Ala480Val Uncertain significance ★★ ⚠ same condition
Built on 18 open, versioned datasets — ClinVar, gnomAD, AlphaMissense, REVEL, ClinGen & more — plus Sugi Variant's own cross-source analysis. Source data 2026-01–2026-10, ClinVar 2026-10. Full sources & versions →
Cite Sugi Variant
Gür T. Sugi Variant: A Deterministic Per-Variant Germline Reference from a Knowledge Graph for Humans and AI Agents. 2026. doi:10.5281/zenodo.21509445. This variant: https://sugi.bio/variant/il17rc-p-val342 (accessed [today's date]).
Preprint & method: sugi.bio/variant/method Machine-readable: this page as Markdown