ClinVar Miner

Submissions for variant NM_007294.4(BRCA1):c.469T>C (p.Ser157Pro)

dbSNP: rs80356897
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV002054876 SCV002462650 likely benign Hereditary breast ovarian cancer syndrome 2023-03-29 criteria provided, single submitter clinical testing
Breast Cancer Information Core (BIC) (BRCA1) RCV000112714 SCV000145592 uncertain significance Breast-ovarian cancer, familial, susceptibility to, 1 2004-11-25 no assertion criteria provided clinical testing

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