ClinVar Miner

Submissions for variant NM_007294.4(BRCA1):c.5312C>G (p.Pro1771Arg)

dbSNP: rs80357025
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV001367865 SCV001564235 likely benign Hereditary breast ovarian cancer syndrome 2023-01-12 criteria provided, single submitter clinical testing
Breast Cancer Information Core (BIC) (BRCA1) RCV000112609 SCV000145447 uncertain significance Breast-ovarian cancer, familial, susceptibility to, 1 2003-12-23 no assertion criteria provided clinical testing
Brotman Baty Institute, University of Washington RCV000112609 SCV001243063 not provided Breast-ovarian cancer, familial, susceptibility to, 1 no assertion provided in vitro

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