ClinVar Miner

Submissions for variant NM_007294.4(BRCA1):c.4899C>T (p.Ser1633=)

dbSNP: rs1567774741
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV001408261 SCV001610257 likely benign Hereditary breast ovarian cancer syndrome 2018-07-09 criteria provided, single submitter clinical testing
Brotman Baty Institute, University of Washington RCV001077275 SCV001243180 not provided Breast-ovarian cancer, familial, susceptibility to, 1 no assertion provided in vitro

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