ClinVar Miner

Submissions for variant NM_000059.3(BRCA2):c.7007G>A (p.Arg2336His) (rs28897743)

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Total submissions: 18
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Ambry Genetics RCV000131031 SCV000185961 pathogenic Hereditary cancer-predisposing syndrome 2018-04-20 criteria provided, single submitter clinical testing Lines of evidence used in support of classification: Last nucleotide of exon,Functionally-validated splicing mutation,Detected in individual satisfying established diagnostic critera for classic disease without a clear mutation
Baylor Genetics RCV000475925 SCV000541005 pathogenic Familial cancer of breast 2017-02-23 criteria provided, single submitter clinical testing
Breast Cancer Information Core (BIC) (BRCA2) RCV000031659 SCV000146991 pathogenic Breast-ovarian cancer, familial 2 2004-02-20 no assertion criteria provided clinical testing
Color RCV000131031 SCV000689020 pathogenic Hereditary cancer-predisposing syndrome 2017-07-26 criteria provided, single submitter clinical testing
Consortium of Investigators of Modifiers of BRCA1/2 (CIMBA), c/o University of Cambridge RCV000031659 SCV000327565 pathogenic Breast-ovarian cancer, familial 2 2015-10-02 criteria provided, single submitter clinical testing
Counsyl RCV000031659 SCV000677695 pathogenic Breast-ovarian cancer, familial 2 2015-06-30 criteria provided, single submitter clinical testing
DNA and Cytogenetics Diagnostics Unit,Erasmus Medical Center RCV000031659 SCV000744505 pathogenic Breast-ovarian cancer, familial 2 2015-09-21 criteria provided, single submitter clinical testing
Department of Pathology and Laboratory Medicine,Sinai Health System RCV000045112 SCV000592088 pathogenic Hereditary breast and ovarian cancer syndrome 2013-01-22 criteria provided, single submitter clinical testing
Diagnostic Laboratory, Department of Genetics,University Medical Center Groningen RCV000031659 SCV000733290 pathogenic Breast-ovarian cancer, familial 2 no assertion criteria provided clinical testing
EGL Genetic Diagnostics,Eurofins Clinical Diagnostics RCV000174440 SCV000225746 pathogenic not provided 2017-06-20 criteria provided, single submitter clinical testing
Foulkes Cancer Genetics LDI, Lady Davis Institute for Medical Research RCV000735595 SCV000863733 pathogenic Breast and/or ovarian cancer 2014-02-10 no assertion criteria provided clinical testing
GeneDx RCV000174440 SCV000210411 pathogenic not provided 2018-01-04 criteria provided, single submitter clinical testing This pathogenic variant is denoted BRCA2 c.7007G>A at the cDNA level. Located at the last nucleotide of exon 13, this variant disrupts a natural splice donor site, and multiple functional studies have found this variant to result in skipping of exon 13 (Thomassen 2006, Sanz 2010, Biswas 2011). Although the nucleotide substitution results in the change of an Arginine to a Histidine at codon 2336, and is called Arg2336His in the literature, we are using only the nucleotide nomenclature to refer to the variant since the defect is determined to be one of splicing rather than a resulting missense variant. BRCA2 c.7007G>A, also denoted 7235G>A using alternate nomenclature, has been identified in both male and female breast cancer patients as well as in the compound heterozygous state or homozygous state in at least five individuals with Fanconi Anemia (Howlett 2002, Alter 2007, Machackova 2008, Ahmad 2012, Coppa 2014, Degrolard-Courcet 2014, Bu 2016, Ghazwani 2016, Lang 2017). This variant was not observed in large population cohorts (Lek 2016). The nucleotide which is altered, a guanine (G) at base 7007, is conserved across species. Based on currently available evidence, we consider this variant to be pathogenic.
Integrated Genetics/Laboratory Corporation of America RCV000045112 SCV000695022 pathogenic Hereditary breast and ovarian cancer syndrome 2016-04-01 criteria provided, single submitter clinical testing Variant Summary: The c.7007G>A variant involves the alteration of a conserved nucleotide and 4/5 in silico tools predict a damaging outcome. The variant affects the last nucleotide of exon 13 and 4/5 splice-site tools predict the variant to affect normal splicing. In silico prediction is confirmed by the in vitro studies that this variant results an aberrant splicing from patient mRNA/cDNA (Sanz_2010, Thomassen_2006, Claes_2004). The variant is absent from the large and broad ExAC control population. The variant has been reported in several HBOC patients in the literature and clinical databases, including the reports of multiple affected individuals from some families indicating the variants cosegregation with the disease. In addition, the variant has also been reported in homozygous or compound heterozygous state in patients with Fanconi anemia. Multiple clinical labs and reputable databases have classified the variant as "pathogenic". Taken together, this variant has been classified as a Pathogenic.
Invitae RCV000045112 SCV000073125 pathogenic Hereditary breast and ovarian cancer syndrome 2018-12-11 criteria provided, single submitter clinical testing This sequence change replaces arginine with histidine at codon 2336 of the BRCA2 protein (p.Arg2336His). The arginine residue is weakly conserved and there is a small physicochemical difference between arginine and histidine. It also falls at the last nucleotide of exon 13 of the BRCA2 coding sequence. This variant is not present in population databases (rs28897743, ExAC no frequency). This variant has been reported in individuals affected with breast and/or ovarian cancer, Fanconia anemia, and acute myelogenous leukemia (PMID: 22486713, 25395318, 12065746, 16115142, 26968956, 22430266). This variant is also known as 7235G>A in the literature. ClinVar contains an entry for this variant (Variation ID: 38077). Experimental studies have shown that this missense change causes skipping of exon 13 (PMID: 16792514, 20215541, 22505045), and fails to rescue the lethal loss of Brca2 in mouse embryonic stem cells (PMID: 21719596). A different variant affecting this nucleotide has been also reported in an individual affected with breast and/or ovarian cancer and caused the skipping of exon 13 (PMID: 22505045), indicating that this nucleotide is crucial for normal mRNA splicing. For these reasons, this variant has been classified as Pathogenic.
OMIM RCV000009923 SCV000030144 pathogenic Fanconi anemia, complementation group D1 2002-07-26 no assertion criteria provided literature only
Quest Diagnostics Nichols Institute San Juan Capistrano RCV000174440 SCV000296656 pathogenic not provided 2016-10-24 criteria provided, single submitter clinical testing
Research Molecular Genetics Laboratory,Women's College Hospital, University of Toronto RCV000045112 SCV000587878 pathogenic Hereditary breast and ovarian cancer syndrome 2014-01-31 no assertion criteria provided research
Sharing Clinical Reports Project (SCRP) RCV000031659 SCV000054266 pathogenic Breast-ovarian cancer, familial 2 2012-10-25 no assertion criteria provided clinical testing

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