NM_001127898.4(CLCN5):c.1251A>G (p.Arg417=) AND Dent disease

Germline classification:: Likely benign (1 submission)
Last evaluated:: Jun 14, 2016
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:: RCV000267166.5

Allele description [Variation Report for NM_001127898.4(CLCN5):c.1251A>G (p.Arg417=)]

NM_001127898.4(CLCN5):c.1251A>G (p.Arg417=)

Gene:

CLCN5:chloride voltage-gated channel 5 [Gene - OMIM - HGNC]

Variant type:

single nucleotide variant

Cytogenetic location:

Xp11.23

Genomic location:

Preferred name:

NM_001127898.4(CLCN5):c.1251A>G (p.Arg417=)

HGVS:

NC_000023.11:g.50086564A>G
NG_007159.3:g.168949A>G
NM_000084.5:c.1041A>G
NM_001127898.4:c.1251A>GMANE SELECT
NM_001127899.4:c.1251A>G
NM_001282163.2:c.1101A>G
NP_000075.1:p.Arg347=
NP_001121370.1:p.Arg417=
NP_001121371.1:p.Arg417=
NP_001269092.1:p.Arg367=
NC_000023.10:g.49851221A>G
NM_000084.3:c.1041A>G

Links:

dbSNP: rs782591993

NCBI 1000 Genomes Browser:

rs782591993

Molecular consequence:

NM_000084.5:c.1041A>G - synonymous variant - [Sequence Ontology: SO:0001819]
NM_001127898.4:c.1251A>G - synonymous variant - [Sequence Ontology: SO:0001819]
NM_001127899.4:c.1251A>G - synonymous variant - [Sequence Ontology: SO:0001819]
NM_001282163.2:c.1101A>G - synonymous variant - [Sequence Ontology: SO:0001819]

Condition(s)

Name:: Dent disease
Synonyms:: Dent's disease
Identifiers:: MONDO: MONDO:0015612; MedGen: C0878681; OMIM: PS300009

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Submission Accession	Submitter	Review Status (Assertion method)	Clinical Significance (Last evaluated)	Origin	Method	Citations
SCV000482542	Illumina Laboratory Services, Illumina	criteria provided, single submitter (ICSL Variant Classification 20161018)	Likely benign (Jun 14, 2016)	germline	clinical testing	PubMed (1) [See all records that cite this PMID] ICSL_Variant_Classification_20161018.pdf Citation Link

Submission Accession

Submitter

Review Status
(Assertion method)

Clinical Significance
(Last evaluated)

Origin

Method

Citations

SCV000482542

Illumina Laboratory Services, Illumina

criteria provided, single submitter

(ICSL Variant Classification 20161018)

Likely benign
(Jun 14, 2016)

germline

clinical testing

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

ICSL_Variant_Classification_20161018.pdf

Citation Link

Help

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

CLCN5 mutation (R347X) associated with hypokalaemic metabolic alkalosis in a Turkish child: an unusual presentation of Dent's disease.

Besbas N, Ozaltin F, Jeck N, Seyberth H, Ludwig M.

Nephrol Dial Transplant. 2005 Jul;20(7):1476-9. Epub 2005 Apr 6. No abstract available.

PubMed [citation]

PMID:: 15814539

Details of each submission

From Illumina Laboratory Services, Illumina, SCV000482542.2

#	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: Apr 9, 2023

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