ClinVar Miner

Submissions for variant NM_000059.3(BRCA2):c.1075G>A (p.Glu359Lys) (rs1555281730)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Color RCV000776715 SCV000912345 uncertain significance Hereditary cancer-predisposing syndrome 2018-08-15 criteria provided, single submitter clinical testing
Donald Williams Parsons Laboratory,Baylor College of Medicine RCV000505644 SCV000599905 other Neuroblastoma 2016-05-01 no assertion criteria provided clinical testing

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