ClinVar Miner

Submissions for variant NM_032043.3(BRIP1):c.2319T>A (p.Asp773Glu)

dbSNP: rs1555590447
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Clinical Genetics Laboratory, Department of Pathology, Netherlands Cancer Institute RCV001694163 SCV001905846 uncertain significance not provided no assertion criteria provided clinical testing
Joint Genome Diagnostic Labs from Nijmegen and Maastricht, Radboudumc and MUMC+ RCV001694163 SCV001955192 uncertain significance not provided no assertion criteria provided clinical testing

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