ClinVar Miner

Submissions for variant NM_007294.3(BRCA1):c.1390_1391insG (p.Thr464fs) (rs397508867)

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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Department of Pathology and Molecular Medicine,Queen's University RCV000496409 SCV000588032 pathogenic Hereditary breast and ovarian cancer syndrome 2017-04-20 criteria provided, single submitter clinical testing
Color RCV000776207 SCV000911353 pathogenic Hereditary cancer-predisposing syndrome 2015-04-10 criteria provided, single submitter clinical testing
Research Molecular Genetics Laboratory,Women's College Hospital, University of Toronto RCV000496409 SCV000587129 pathogenic Hereditary breast and ovarian cancer syndrome 2014-01-31 no assertion criteria provided research

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