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IL17RC p.Pro559Ser

c.1675C>T · rs749511204 · VCV1393904

Uncertain significance Single submitter
Classification
Uncertain significance
ClinVar
Review
Single submitter ★☆☆☆
ClinVar · 1 submitter
AlphaMissense
likely benign
0.1995 · ACMG-weighted
gnomAD v4.1
Not reported
no allele count reported in gnomAD v4.1 (AN 1,577,048)
Missense predictors
0/3 damaging
AlphaMissense, REVEL, SaProt
Conditions
1
candidiasis, familial, 9

Computational evidence

Protein change
AlphaMissense0.1995likely benign
REVEL0.067moderately benign-leaning
SaProtLLR -9.87tolerated
⇒ AlphaMissense, REVEL and SaProt all call this tolerated.
Splicing
SpliceAI—not assessed · no allele here is in the release
Constraint at this position
ConservationphyloP 0.17GERP -2.7, phastCons 0.002
Regional constrainto/e 1.02unconstrained · MANE · 16 kb · p 0.58 · regional, not allelic
Overall
CADD16.27PHRED · 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

gnomAD v4.1 · exomes + genomes

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
Full IL17RC gene report on Sugi Atlas → Gene function, pathways, protein structure, interactions & more

Disease context

candidiasis, familial, 9 — disease report on Sugi Atlas → Associated genes, phenotypes, clinical trials & treatments

For Chronic mucocutaneous candidiasis (Orphanet):

Inheritance
Autosomal dominant, Autosomal recessive
Onset
Childhood, Infancy

Similar variants

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