ClinVar Miner

Submissions for variant NM_000059.3(BRCA2):c.5247T>G (p.Tyr1749Ter)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Color RCV000775314 SCV000909573 pathogenic Hereditary cancer-predisposing syndrome 2018-05-07 criteria provided, single submitter clinical testing
Core Molecular Diagnostic Lab,McGill University Health Centre RCV000722069 SCV000852057 likely pathogenic Breast-ovarian cancer, familial 2 2018-11-13 criteria provided, single submitter clinical testing

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