IL17RC p.Pro559Ser
c.1675C>T · rs749511204 · VCV1393904
Computational evidence
| Protein change | ||
| AlphaMissense | 0.1995 | likely benign |
|---|---|---|
| REVEL | 0.067 | moderately benign-leaning |
| SaProt | LLR -9.87 | tolerated |
| ⇒ AlphaMissense, REVEL and SaProt all call this tolerated. | ||
| Splicing | ||
| SpliceAI | — | not assessed · no allele here is in the release |
| Constraint at this position | ||
| Conservation | phyloP 0.17 | GERP -2.7, phastCons 0.002 |
| Regional constraint | o/e 1.02 | unconstrained · MANE · 16 kb · p 0.58 · regional, not allelic |
| Overall | ||
| CADD | 16.27 | PHRED · no single calibrated threshold — expert panels disagree |
ClinVar classifies this uncertain; the computational predictors unanimously lean tolerated — a triage signal, not a reclassification
AlphaMissense carries the ACMG weight for missense; REVEL and SaProt are independent agreement signals.
⚠ Isoform check: AlphaMissense numbered on a different transcript (AM P630S vs ClinVar P559S) — verify the residue.
Population frequency
No allele count reported in gnomAD v4.1 (AN 1,577,048). This is missing data, not an absence: the variant may or may not be present in gnomAD. Rarity (ACMG PM2) and BA1/BS1 cannot be assessed for it.
Variant & gene context
- Gene
- IL17RC
- Protein
- p.Pro559Ser
- Coding
- c.1675C>T
- MANE Select
- NM_153460
- dbSNP
- rs749511204
- Type
- single nucleotide variant
- Location
- chr3:9933105 (GRCh38)
- Gene constraint
- LOEUF 0.777 · pLI <0.01 (gnomAD)
- Structure
- AlphaFold pLDDT 74.19 · 5 PDB
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 p.Pro559fs Conflicting classifications of pathogenicity ★ same residue
- 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
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-pro559ser (accessed [today's date]).
Preprint & method: sugi.bio/variant/method Machine-readable: this page as Markdown