ClinVar Miner

Submissions for variant NM_007294.3(BRCA1):c.5258G>C (p.Arg1753Thr) (rs397509246)

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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
ClinVar Staff, National Center for Biotechnology Information (NCBI) RCV000577271 SCV000679296 not provided Familial cancer of breast no assertion provided literature only
Color RCV000771309 SCV000903565 uncertain significance Hereditary cancer-predisposing syndrome 2018-05-28 criteria provided, single submitter clinical testing
Quest Diagnostics Nichols Institute San Juan Capistrano RCV000759559 SCV000888945 likely pathogenic not provided 2018-03-07 criteria provided, single submitter clinical testing

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