ClinVar Miner

Submissions for variant NM_000059.3(BRCA2):c.8300C>G (p.Pro2767Arg) (rs397507401)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Integrated Genetics/Laboratory Corporation of America RCV000781150 SCV000919020 uncertain significance not specified 2018-10-22 criteria provided, single submitter clinical testing Variant summary: BRCA2 c.8300C>G (p.Pro2767Arg) results in a non-conservative amino acid change located in the BRCA2, OB1 domain of the encoded protein sequence. Five of five in-silico tools predict a damaging effect of the variant on protein function. The variant was absent in 243212 control chromosomes. c.8300C>G has been reported in the literature in one individual affected with Hereditary Breast and Ovarian Cancer without strong evidence for or against causality. Thus, this report does not provide unequivocal conclusions about association of the variant with Hereditary Breast and Ovarian Cancer. To our knowledge, no experimental evidence demonstrating an impact on protein function has been reported. No clinical diagnostic laboratories have submitted clinical-significance assessments for this variant to ClinVar after 2014. Based on the evidence outlined above, the variant was classified as uncertain significance.
Sharing Clinical Reports Project (SCRP) RCV000031733 SCV000054340 uncertain significance Breast-ovarian cancer, familial 2 2009-03-24 no assertion criteria provided clinical testing

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