ClinVar Miner

Submissions for variant NM_000059.4(BRCA2):c.8414T>C (p.Leu2805Ser)

gnomAD frequency: 0.00001  dbSNP: rs397507983
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Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
ClinVar Staff, National Center for Biotechnology Information (NCBI) RCV000576922 SCV000678941 not provided Familial cancer of breast no assertion provided literature only
Clinical Genetics Laboratory, Department of Pathology, Netherlands Cancer Institute RCV001689604 SCV001906321 uncertain significance not provided no assertion criteria provided clinical testing
Joint Genome Diagnostic Labs from Nijmegen and Maastricht, Radboudumc and MUMC+ RCV001689604 SCV001951288 uncertain significance not provided no assertion criteria provided clinical testing
Clinical Genetics DNA and cytogenetics Diagnostics Lab, Erasmus MC, Erasmus Medical Center RCV001689604 SCV001980293 uncertain significance not provided no assertion criteria provided clinical testing

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