ClinVar Miner

Submissions for variant NM_007294.4(BRCA1):c.5153G>T (p.Trp1718Leu)

dbSNP: rs41293461
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Hereditary Cancer Genetics group, Vall d'Hebron Institute of Oncology RCV000845277 SCV000916356 uncertain significance Hereditary breast ovarian cancer syndrome 2019-03-01 no assertion criteria provided research
Brotman Baty Institute, University of Washington RCV001072409 SCV001237784 not provided Breast-ovarian cancer, familial, susceptibility to, 1 no assertion provided in vitro

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