Is CCDC40 p.Lys952fs (c.2852dup) pathogenic?

CCDC40 p.Lys952fs (c.2852dup) is classified Pathogenic in CCDC40 (ClinVar, Multiple submitters, 2 submitters; last evaluated 2017-12-27). Very rare (popmax 0.000339%, nfe); Associated with primary ciliary dyskinesia.

What condition is associated with CCDC40 p.Lys952fs (c.2852dup)?

CCDC40 p.Lys952fs (c.2852dup) is associated with primary ciliary dyskinesia (ClinVar).

How common is CCDC40 p.Lys952fs (c.2852dup) in the general population?

CCDC40 p.Lys952fs (c.2852dup) is very rare (popmax 0.000339%, nfe) (gnomAD).

How is Primary ciliary dyskinesia inherited?

Typically Autosomal dominant, Autosomal recessive (Orphanet). A genetic counselor can assess individual risk for a family.

CCDC40 p.Lys952fs

c.2852dup · rs878855042 · VCV241240

Pathogenic Multiple submitters

Classification

Pathogenic

ClinVar

Review

Multiple submitters ★★☆☆

ClinVar · 2 submitters

Consequence

frameshift

predicted LoF

gnomAD v4.1

Rare

very rare (popmax 0.000339%, nfe)

Conditions

primary ciliary dyskinesia

Computational evidence

Protein change
Missense predictors do not apply to this variant type; conservation carries the signal.
Consequence	frameshift	predicted loss-of-function
NMD	predicted	premature termination codon in exon 18 of 20
Splicing
SpliceAI	—	not assessed · substitutions only
Constraint at this position
Conservation	phyloP 1.3	GERP -1, phastCons 1

Predicted loss-of-function is descriptive, not an applied PVS1 code.

Population frequency

gnomAD v4.1 · exomes + genomes

Grpmax group 0.000339% European (non-Finnish) · 4/1,180,032 alleles

Filtering AF 7.9e-05% ClinGen BA1/BS1 input FAF95, joint · FAF99 5.4e-05%

Overall 0.000274% 4/1,461,558 alleles · very rare

Rarity supports pathogenicity (ACMG PM2); frequency above a disease-specific BA1/BS1 threshold argues against it. A variant frequent in one ancestry group can be near-absent in others, so a single global figure can mislead.

Variant & gene context

Gene: CCDC40
Protein: p.Lys952fs
Coding: c.2852dup
MANE Select: NM_017950
dbSNP: rs878855042
Type: Duplication
Location: chr17:80095281 (GRCh38)
Gene constraint: LOEUF 0.962 · pLI <0.01 · ClinGen HI gene assoc. with recessive phenotype (gnomAD)
Structure: AlphaFold pLDDT 71.70 · 1 PDB

Full CCDC40 gene report on Sugi Atlas → Gene function, pathways, protein structure, interactions & more

Disease context

primary ciliary dyskinesia — disease report on Sugi Atlas → Associated genes, phenotypes, clinical trials & treatments

For Primary ciliary dyskinesia (Orphanet):

Inheritance: Autosomal dominant, Autosomal recessive, X-linked recessive
Onset: Neonatal
Prevalence: 1-5 / 10 000 (Pakistan)

Similar variants

CCDC40 p.Asn887fs Pathogenic/Likely pathogenic ★★ same condition
CCDC40 p.Ile1002fs Pathogenic ★★ same condition
CCDC40 p.Arg359fs Pathogenic ★ same condition
CCDC40 p.Arg412fs Pathogenic ★ same condition
CCDC40 p.Asp982fs Pathogenic ★ same condition
CCDC40 p.Glu1096fs Pathogenic ★ same condition
CCDC40 p.Met833fs Pathogenic ★ same condition
CCDC40 p.Phe141fs Pathogenic ★ 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/ccdc40-p-lys952fs (accessed [today's date]).

Preprint & method: sugi.bio/variant/method Machine-readable: this page as Markdown