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NM_007194.4(CHEK2):c.319+39dup AND not provided

Germline classification:
Benign (1 submission)
Last evaluated:
Jun 23, 2018
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:
RCV001707870.2

Allele description [Variation Report for NM_007194.4(CHEK2):c.319+39dup]

NM_007194.4(CHEK2):c.319+39dup

Gene:
CHEK2:checkpoint kinase 2 [Gene - OMIM - HGNC]
Variant type:
Duplication
Cytogenetic location:
22q12.1
Genomic location:
Preferred name:
NM_007194.4(CHEK2):c.319+39dup
HGVS:
  • NC_000022.11:g.28734364dup
  • NG_008150.2:g.12507dup
  • NM_001005735.2:c.319+39dup
  • NM_001257387.2:c.-459+39dup
  • NM_001349956.2:c.319+39dup
  • NM_007194.4:c.319+39dupMANE SELECT
  • NM_145862.2:c.319+39dup
  • LRG_302t1:c.319+39dup
  • LRG_302:g.12507dup
  • NC_000022.10:g.29130347_29130348insT
  • NC_000022.10:g.29130352dup
  • NM_007194.4:c.319+43dupMANE SELECT
Links:
dbSNP: rs3841692
NCBI 1000 Genomes Browser:
rs3841692
Molecular consequence:
  • NM_001005735.2:c.319+39dup - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001257387.2:c.-459+39dup - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001349956.2:c.319+39dup - intron variant - [Sequence Ontology: SO:0001627]
  • NM_007194.4:c.319+39dup - intron variant - [Sequence Ontology: SO:0001627]
  • NM_145862.2:c.319+39dup - intron variant - [Sequence Ontology: SO:0001627]

Condition(s)

Synonyms:
none provided
Identifiers:
MedGen: C3661900

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Assertion and evidence details

Help
Submission AccessionSubmitterReview Status
(Assertion method)		Clinical Significance
(Last evaluated)		OriginMethodCitations
SCV001935625GeneDx
criteria provided, single submitter

(GeneDx Variant Classification Process June 2021)		Benign
(Jun 23, 2018) 		germlineclinical testing

Citation Link

Help

Summary from all submissions

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

Details of each submission

From GeneDx, SCV001935625.1

#EthnicityIndividualsChromosomes TestedFamily HistoryMethodCitations
1not providednot providednot providednot providedclinical testingnot provided

Description

This variant is associated with the following publications: (PMID: 26506619)

#SampleMethodObservation
OriginAffectedNumber testedTissuePurposeMethodIndividualsAllele frequencyFamiliesCo-occurrences
1germlineyesnot providednot providednot providednot providednot providednot providednot provided

Last Updated: Sep 29, 2024