Is DNAH5 p.Glu3380= (c.10140A>G) pathogenic?

DNAH5 p.Glu3380= (c.10140A>G) is classified Benign/Likely benign in DNAH5 (ClinVar, Multiple submitters, 12 submitters; last evaluated 2026-02-04). Common (popmax 43.4%, sas) — too common for a highly-penetrant pathogenic allele; Associated with primary ciliary dyskinesia.

What condition is associated with DNAH5 p.Glu3380= (c.10140A>G)?

DNAH5 p.Glu3380= (c.10140A>G) is associated with primary ciliary dyskinesia, primary ciliary dyskinesia 3 (ClinVar).

How is Primary ciliary dyskinesia inherited?

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

DNAH5 p.Glu3380=

Q: How common is DNAH5 p.Glu3380= (c.10140A>G) in the general population?

DNAH5 p.Glu3380= (c.10140A>G) is common (popmax 43.4%, sas) — too common for a highly-penetrant pathogenic allele (gnomAD).

c.10140A>G · rs6554812 · VCV163137

Benign/Likely benign Multiple submitters

Classification

Benign/Likely benign

ClinVar

Review

Multiple submitters ★★☆☆

ClinVar · 12 submitters

gnomAD v4.1

Common

common (popmax 43.4%, sas) — too common for a highly-penetrant pathogenic allele

Conditions

primary ciliary dyskinesia

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 -2.3	GERP -5.3
Overall
CADD	1.16	PHRED · no single calibrated threshold — expert panels disagree

Population frequency

gnomAD v4.1 · exomes + genomes

Grpmax group 43.4% South Asian · 39,546/91,042 alleles

Filtering AF 43.1% ClinGen BA1/BS1 input FAF95, joint · FAF99 42.9%

Overall 28.2% 455,168/1,612,358 alleles · common

Ancestry group	Frequency	1 in
South Asiangrpmax	43.4%	2
Finnishnot grpmax-eligible	41.6%	2
African / African-American	36.7%	3
Admixed American	28.8%	3
Remaining individualsnot grpmax-eligible	27.6%	4
European (non-Finnish)	26.7%	4
Middle Eastern	22.5%	4
Ashkenazi Jewishnot grpmax-eligible	20.8%	5
Amishnot grpmax-eligible	15.6%	6
East Asian	10.5%	10

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: DNAH5
Protein: p.Glu3380=
Coding: c.10140A>G
MANE Select: NM_001369
dbSNP: rs6554812
Type: single nucleotide variant
Location: chr5:13762863 (GRCh38)
Gene constraint: LOEUF 0.764 · pLI <0.01 · ClinGen HI gene assoc. with recessive phenotype (gnomAD)
Residue 3380: the 'stalk' region

Full DNAH5 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

Also linked: primary ciliary dyskinesia 3

For Primary ciliary dyskinesia (Orphanet):

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

Similar variants

DNAH5 p.Glu3380Ter Pathogenic ★ same residue
DNAH5 c.10555+1G>C Likely pathogenic ★★ same condition
DNAH5 c.1089+1G>A Pathogenic ★★ same condition
DNAH5 c.11028+2T>C Pathogenic/Likely pathogenic ★★ same condition
DNAH5 c.11029-2A>T Pathogenic/Likely pathogenic ★★ same condition
DNAH5 c.11571-1G>A Pathogenic ★★ same condition
DNAH5 c.12910-1G>C Pathogenic/Likely pathogenic ★★ same condition
DNAH5 c.1320+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/dnah5-p-glu3380 (accessed [today's date]).

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