ClinVar Miner

Submissions for variant NM_007294.4(BRCA1):c.4356del (p.Ala1453fs)

dbSNP: rs1567782959
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Department of Molecular Diagnostics, Institute of Oncology Ljubljana RCV000754612 SCV000864197 likely pathogenic Breast-ovarian cancer, familial, susceptibility to, 1 2019-01-11 criteria provided, single submitter clinical testing
CeGaT Center for Human Genetics Tuebingen RCV002275143 SCV002563413 pathogenic not provided 2019-06-01 criteria provided, single submitter clinical testing

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