ClinVar Miner

Submissions for variant NM_007294.4(BRCA1):c.5513T>G (p.Val1838Gly)

dbSNP: rs80357107
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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 Medical Genetics, Oslo University Hospital RCV000241502 SCV000564325 likely pathogenic Breast-ovarian cancer, familial, susceptibility to, 1 2015-07-01 criteria provided, single submitter clinical testing
Department of Medical Genetics, University Hospital of North Norway RCV000241502 SCV000301441 uncertain significance Breast-ovarian cancer, familial, susceptibility to, 1 2016-05-01 no assertion criteria provided clinical testing
Brotman Baty Institute, University of Washington RCV000241502 SCV001237607 not provided Breast-ovarian cancer, familial, susceptibility to, 1 no assertion provided in vitro

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