NM_181426.2(CCDC39):c.1528-43A>G AND Primary ciliary dyskinesia

This record was updated by the submitter. Please see the current version.

Germline classification:: Benign (1 submission)
Last evaluated:: Nov 28, 2023
Review status:: 1 star out of maximum of 4 stars
criteria provided, single submitter

Somatic classification of clinical impact:: None
Review status:: (0/4) 0 stars out of maximum of 4 stars
no assertion criteria provided

Somatic classification of oncogenicity:: None
Review status:: (0/4) 0 stars out of maximum of 4 stars
no assertion criteria provided

Record status:: current
Accession:: RCV001510184.6

Allele description

NM_181426.2(CCDC39):c.1528-43A>G

Gene:

CCDC39:coiled-coil domain 39 molecular ruler complex subunit [Gene - OMIM - HGNC]

Variant type:

single nucleotide variant

Cytogenetic location:

3q26.33

Genomic location:

Preferred name:

NM_181426.2(CCDC39):c.1528-43A>G

HGVS:

NC_000003.12:g.180644300T>C
NG_029581.1:g.40196A>G
NM_181426.2:c.1528-43A>GMANE SELECT
NC_000003.11:g.180362088T>C
NM_181426.1:c.1528-43A>G

Links:

dbSNP: rs73051767

NCBI 1000 Genomes Browser:

rs73051767

Molecular consequence:

NM_181426.2:c.1528-43A>G - intron variant - [Sequence Ontology: SO:0001627]

Condition(s)

Name:: Primary ciliary dyskinesia
Synonyms:: Ciliary dyskinesia
Identifiers:: MONDO: MONDO:0016575; MedGen: C0008780; OMIM: PS244400; Human Phenotype Ontology: HP:0012265

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Gene Links for GEO Profiles (Select 79325306) (1)
Gene
Homologene neighbors for GEO Profiles (Select 79323154) (0)
GEO Profiles
UBR4 ubiquitin protein ligase E3 component n-recognin 4 [Homo sapiens]
UBR4 ubiquitin protein ligase E3 component n-recognin 4 [Homo sapiens]
Gene ID:23352

Gene
Wildfire-Impacted Soil and Aquatic Microbiomes
Wildfire-Impacted Soil and Aquatic Microbiomes
Wildfire-Impacted Soil and Aquatic Microbiomes Metagenome

BioProject
BioProject Links for BioSample (Select 35300609) (1)
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Submission Accession	Submitter	Review Status (Assertion method)	Clinical Significance (Last evaluated)	Origin	Method	Citations
SCV001717150	Invitae	criteria provided, single submitter (Invitae Variant Classification Sherloc (09022015))	Benign (Nov 28, 2023)	germline	clinical testing	PubMed (1) [See all records that cite this PMID]

Submission Accession

Submitter

Review Status
(Assertion method)

Clinical Significance
(Last evaluated)

Origin

Method

Citations

SCV001717150

Invitae

criteria provided, single submitter

(Invitae Variant Classification Sherloc (09022015))

Benign
(Nov 28, 2023)

germline

clinical testing

PubMed (1)
[See all records that cite this PMID]

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Summary from all submissions

Ethnicity	Origin	Affected	Individuals	Families	Chromosomes tested	Number Tested	Family history	Method
not provided	germline	unknown	not provided	not provided	not provided	not provided	not provided	clinical testing

Citations

PubMed

Sherloc: a comprehensive refinement of the ACMG-AMP variant classification criteria.

Nykamp K, Anderson M, Powers M, Garcia J, Herrera B, Ho YY, Kobayashi Y, Patil N, Thusberg J, Westbrook M; Invitae Clinical Genomics Group., Topper S.

Genet Med. 2017 Oct;19(10):1105-1117. doi: 10.1038/gim.2017.37. Epub 2017 May 11. Erratum in: Genet Med. 2020 Jan;22(1):240. doi: 10.1038/s41436-019-0624-9.

PubMed [citation]

PMID:: 28492532
PMCID:: PMC5632818

Details of each submission

From Invitae, SCV001717150.3

#	Ethnicity	Individuals	Chromosomes Tested	Family History	Method	Citations
1	not provided	not provided	not provided	not provided	clinical testing	PubMed (1)

#	Sample				Method		Observation
#	Origin	Affected	Number tested	Tissue	Purpose	Method	Individuals	Allele frequency	Families	Co-occurrences
1	germline	unknown	not provided	not provided	not provided		not provided	not provided	not provided	not provided

Last Updated: Sep 16, 2024

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