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NM_007194.4(CHEK2):c.77C>A (p.Thr26Asn) AND Hereditary cancer-predisposing syndrome

Germline classification:
Uncertain significance (1 submission)
Last evaluated:
Sep 20, 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:
RCV002411054.2

Allele description [Variation Report for NM_007194.4(CHEK2):c.77C>A (p.Thr26Asn)]

NM_007194.4(CHEK2):c.77C>A (p.Thr26Asn)

Gene:
CHEK2:checkpoint kinase 2 [Gene - OMIM - HGNC]
Variant type:
single nucleotide variant
Cytogenetic location:
22q12.1
Genomic location:
Preferred name:
NM_007194.4(CHEK2):c.77C>A (p.Thr26Asn)
HGVS:
  • NC_000022.11:g.28734645G>T
  • NG_008150.2:g.12222C>A
  • NM_001005735.2:c.77C>A
  • NM_001257387.2:c.-701C>A
  • NM_001349956.2:c.77C>A
  • NM_007194.4:c.77C>AMANE SELECT
  • NM_145862.2:c.77C>A
  • NP_001005735.1:p.Thr26Asn
  • NP_001336885.1:p.Thr26Asn
  • NP_009125.1:p.Thr26Asn
  • NP_665861.1:p.Thr26Asn
  • LRG_302t1:c.77C>A
  • LRG_302:g.12222C>A
  • LRG_302p1:p.Thr26Asn
  • NC_000022.10:g.29130633G>T
  • NG_008150.1:g.12190C>A
  • NM_007194.3:c.77C>A
Protein change:
T26N
Links:
dbSNP: rs878854923
NCBI 1000 Genomes Browser:
rs878854923
Molecular consequence:
  • NM_001257387.2:c.-701C>A - 5 prime UTR variant - [Sequence Ontology: SO:0001623]
  • NM_001005735.2:c.77C>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001349956.2:c.77C>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_007194.4:c.77C>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_145862.2:c.77C>A - missense variant - [Sequence Ontology: SO:0001583]

Condition(s)

Name:
Hereditary cancer-predisposing syndrome
Synonyms:
Neoplastic Syndromes, Hereditary; Tumor predisposition; Cancer predisposition; See all synonyms [MedGen]
Identifiers:
MONDO: MONDO:0015356; MeSH: D009386; MedGen: C0027672

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Assertion and evidence details

Help
Submission AccessionSubmitterReview Status
(Assertion method)		Clinical Significance
(Last evaluated)		OriginMethodCitations
SCV002673297Ambry Genetics
criteria provided, single submitter

(Ambry Variant Classification Scheme 2023)		Uncertain significance
(Sep 20, 2018) 		germlineclinical testing

Citation Link

Help

Summary from all submissions

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

Details of each submission

From Ambry Genetics, SCV002673297.2

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

Description

The p.T26N variant (also known as c.77C>A), located in coding exon 1 of the CHEK2 gene, results from a C to A substitution at nucleotide position 77. The threonine at codon 26 is replaced by asparagine, an amino acid with similar properties. This amino acid position is poorly conserved in available vertebrate species. In addition, this alteration is predicted to be tolerated by in silico analysis. Since supporting evidence is limited at this time, the clinical significance of this alteration remains unclear.

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

Last Updated: Sep 29, 2024