ClinVar Miner

Submissions for variant NM_007294.4(BRCA1):c.56A>G (p.Gln19Arg)

dbSNP: rs2055725680
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV001071148 SCV001236436 uncertain significance Hereditary breast ovarian cancer syndrome 2019-04-10 criteria provided, single submitter clinical testing In summary, the available evidence is currently insufficient to determine the role of this variant in disease. Therefore, it has been classified as a Variant of Uncertain Significance. This variant has been reported not to substantially affect BRCA1 protein function (PMID: 30209399). This variant has not been reported in the literature in individuals with BRCA1-related conditions. This variant is not present in population databases (ExAC no frequency). This sequence change replaces glutamine with arginine at codon 19 of the BRCA1 protein (p.Gln19Arg). The glutamine residue is highly conserved and there is a small physicochemical difference between glutamine and arginine.
Brotman Baty Institute, University of Washington RCV001076482 SCV001242246 not provided Breast-ovarian cancer, familial, susceptibility to, 1 no assertion provided in vitro

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