ClinVar Miner

Submissions for variant NM_000059.3(BRCA2):c.598A>G (p.Thr200Ala) (rs398122543)

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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Ambry Genetics RCV000221268 SCV000272999 uncertain significance Hereditary cancer-predisposing syndrome 2014-11-20 criteria provided, single submitter clinical testing
Color RCV000221268 SCV000905900 uncertain significance Hereditary cancer-predisposing syndrome 2018-10-11 criteria provided, single submitter clinical testing
Sharing Clinical Reports Project (SCRP) RCV000076949 SCV000108746 uncertain significance Breast-ovarian cancer, familial 2 2008-04-09 no assertion criteria provided clinical testing

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