ClinVar Miner

Submissions for variant NM_000059.3(BRCA2):c.9391T>C (p.Ser3131Pro) (rs398122613)

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Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Ambry Genetics RCV000218620 SCV000273382 uncertain significance Hereditary cancer-predisposing syndrome 2016-06-01 criteria provided, single submitter clinical testing Lines of evidence used in support of classification: Insufficient or conflicting evidence
Quest Diagnostics Nichols Institute San Juan Capistrano RCV000506488 SCV000600860 uncertain significance not specified 2017-04-08 criteria provided, single submitter clinical testing
Color RCV000218620 SCV000906701 uncertain significance Hereditary cancer-predisposing syndrome 2018-06-13 criteria provided, single submitter clinical testing
Sharing Clinical Reports Project (SCRP) RCV000077041 SCV000108838 uncertain significance Breast-ovarian cancer, familial 2 2012-10-03 no assertion criteria provided clinical testing

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