ClinVar Miner

Submissions for variant NM_007294.4(BRCA1):c.34C>G (p.Gln12Glu)

dbSNP: rs80357134
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV000801423 SCV000941198 uncertain significance Hereditary breast ovarian cancer syndrome 2018-09-06 criteria provided, single submitter clinical testing Algorithms developed to predict the effect of missense changes on protein structure and function are either unavailable or do not agree on the potential impact of this missense change (SIFT: "Tolerated"; PolyPhen-2: "Probably Damaging"; Align-GVGD: "Class C0"). This variant has been reported in individuals in the Leiden Open-source Variation Database (PMID: 21520333). This variant is not present in population databases (ExAC no frequency). This sequence change replaces glutamine with glutamic acid at codon 12 of the BRCA1 protein (p.Gln12Glu). The glutamine residue is moderately conserved and there is a small physicochemical difference between glutamine and glutamic acid. 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.
Brotman Baty Institute, University of Washington RCV001076453 SCV001242212 not provided Breast-ovarian cancer, familial, susceptibility to, 1 no assertion provided in vitro

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