Is CCDC39 p.Phe403fs (c.1208_1209insGGTGTGCTGT…[124 bp]) pathogenic?

CCDC39 p.Phe403fs (c.12081209insGGTGTGCTGT…[124 bp]) is classified Pathogenic in CCDC39 (ClinVar, Single submitter, 1 submitter; last evaluated 2014-12-05). No gnomAD frequency available for this variant; Associated with primary ciliary dyskinesia.

What condition is associated with CCDC39 p.Phe403fs (c.1208_1209insGGTGTGCTGT…[124 bp])?

CCDC39 p.Phe403fs (c.1208_1209insGGTGTGCTGT…[124 bp]) is associated with primary ciliary dyskinesia (ClinVar).

How common is CCDC39 p.Phe403fs (c.1208_1209insGGTGTGCTGT…[124 bp]) in the general population?

CCDC39 p.Phe403fs (c.1208_1209insGGTGTGCTGT…[124 bp]) is no gnomAD frequency available for this variant (gnomAD).

How is Primary ciliary dyskinesia inherited?

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

CCDC39 p.Phe403fs

c.1208_1209insGGTGTGCTGT…[124 bp] · rs2108421980 · VCV1073617

Pathogenic Single submitter

Classification

Pathogenic

ClinVar

Review

Single submitter ★☆☆☆

ClinVar · 1 submitter

Consequence

frameshift

predicted LoF

gnomAD v4.1

Not reported

no gnomAD frequency available for this variant

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 10 of 20
Splicing
SpliceAI	—	not assessed · substitutions only
Constraint at this position
Conservation	phyloP 3	GERP -2.4, phastCons 1

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

Population frequency

dbSNP / gnomAD

No gnomAD frequency available for this variant. 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: CCDC39
Protein: p.Phe403fs
Coding: c.1208_1209insGGTGTGCTGTTGCGTGAACCTGGGAGGCGGAGCTTGCAGTGAGCCGAGATCGCGCCACTGCACTCCAGCCTGGGCGACAGAGCGAGACTCCGTCTCAAAAAAAAAAAAAAAAAGGTGTGCTGTT
MANE Select: NM_181426
dbSNP: rs2108421980
Type: Insertion
Location: chr3:180648318 (GRCh38)
Gene constraint: LOEUF 1.226 · pLI <0.01 · ClinGen HI gene assoc. with recessive phenotype (gnomAD)
Structure: AlphaFold pLDDT 79.23 · 1 PDB

Full CCDC39 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

CCDC39 p.His340fs Pathogenic/Likely pathogenic ★★ same condition
CCDC39 p.Ile224Ter Pathogenic ★ same condition
CCDC39 p.Leu420fs Pathogenic ★ same condition
CCDC39 c.1363-12_1363-11insT Likely benign ★ same condition
CCDC39 c.1363-17_1363-16insC Likely benign ★ same condition
CCDC39 c.1034+2T>A Pathogenic/Likely pathogenic ★★ same condition
CCDC39 c.1167+1261A>G Pathogenic/Likely pathogenic ★★ same condition
CCDC39 c.1362+1G>A Likely 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/ccdc39-p-phe403fs (accessed [today's date]).

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