ClinVar Miner

Submissions for variant NM_032043.3(BRIP1):c.2571dup (p.Ser858fs)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Institute of Human Genetics, University of Leipzig Medical Center RCV005247945 SCV005900191 pathogenic Familial cancer of breast 2025-03-04 criteria provided, single submitter clinical testing Criteria applied: PVS1,PM2_MOD

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