ClinVar Miner

Submissions for variant NM_007294.3(BRCA1):c.5365G>T (p.Ala1789Ser) (rs80357078)

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Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Breast Cancer Information Core (BIC) (BRCA1) RCV000112629 SCV000145483 uncertain significance Breast-ovarian cancer, familial 1 2003-12-23 no assertion criteria provided clinical testing
Color RCV000580957 SCV000683306 uncertain significance Hereditary cancer-predisposing syndrome 2018-08-21 criteria provided, single submitter clinical testing
Counsyl RCV000112629 SCV000785154 uncertain significance Breast-ovarian cancer, familial 1 2017-05-09 criteria provided, single submitter clinical testing
DNA and Cytogenetics Diagnostics Unit,Erasmus Medical Center RCV000112629 SCV000744585 likely benign Breast-ovarian cancer, familial 1 2015-09-21 criteria provided, single submitter clinical testing

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