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NM_000083.3(CLCN1):c.562+5G>C AND Congenital myotonia, autosomal dominant form

Germline classification:
Uncertain significance (1 submission)
Last evaluated:
Nov 24, 2023
Review status:
(0/4) 0 stars out of maximum of 4 stars
no assertion criteria provided
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:
RCV003444482.1

Allele description [Variation Report for NM_000083.3(CLCN1):c.562+5G>C]

NM_000083.3(CLCN1):c.562+5G>C

Gene:
CLCN1:chloride voltage-gated channel 1 [Gene - OMIM - HGNC]
Variant type:
single nucleotide variant
Cytogenetic location:
7q34
Genomic location:
Preferred name:
NM_000083.3(CLCN1):c.562+5G>C
HGVS:
  • NC_000007.14:g.143321498G>C
  • NG_009815.2:g.10373G>C
  • NM_000083.3:c.562+5G>CMANE SELECT
  • NC_000007.13:g.143018591G>C
Molecular consequence:
  • NM_000083.3:c.562+5G>C - intron variant - [Sequence Ontology: SO:0001627]

Condition(s)

Name:
Congenital myotonia, autosomal dominant form (THD)
Synonyms:
Myotonia congenita autosomal dominant; Thomsen disease; Thomsen's disease
Identifiers:
MONDO: MONDO:0008055; MedGen: C2936781; Orphanet: 614; OMIM: 160800

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Assertion and evidence details

Submission AccessionSubmitterReview Status
(Assertion method)
Clinical Significance
(Last evaluated)
OriginMethodCitations
SCV004171590Zotz-Klimas Genetics Lab, MVZ Zotz Klimas
no assertion criteria provided
Uncertain significance
(Nov 24, 2023)
germlineclinical testing

Summary from all submissions

EthnicityOriginAffectedIndividualsFamiliesChromosomes testedNumber TestedFamily historyMethod
not providedgermlineyesnot providednot providednot providednot providednot providedclinical testing

Details of each submission

From Zotz-Klimas Genetics Lab, MVZ Zotz Klimas, SCV004171590.1

#EthnicityIndividualsChromosomes TestedFamily HistoryMethodCitations
1not providednot providednot providednot providedclinical testingnot provided
#SampleMethodObservation
OriginAffectedNumber testedTissuePurposeMethodIndividualsAllele frequencyFamiliesCo-occurrences
1germlineyesnot providednot providednot providednot providednot providednot providednot provided

Last Updated: Dec 9, 2023