ClinVar Miner

Submissions for variant NM_007294.4(BRCA1):c.5282T>G (p.Phe1761Cys)

dbSNP: rs80356905
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Quest Diagnostics Nichols Institute San Juan Capistrano RCV000508677 SCV000605912 uncertain significance not specified 2016-12-08 criteria provided, single submitter clinical testing
Breast Center, Key Laboratory of Carcinogenesis and Translational Research RCV001254335 SCV001430319 likely pathogenic Hereditary breast ovarian cancer syndrome 2020-05-01 criteria provided, single submitter clinical testing
Brotman Baty Institute, University of Washington RCV001076012 SCV001241684 not provided Breast-ovarian cancer, familial, susceptibility to, 1 no assertion provided in vitro

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