ClinVar Miner

Submissions for variant NM_000059.3(BRCA2):c.1077A>G (p.Glu359=) (rs1135401832)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Cancer Genetics and Genomics Laboratory,British Columbia Cancer Agency RCV000496538 SCV000586923 uncertain significance Hereditary breast and ovarian cancer syndrome 2016-04-14 no assertion criteria provided clinical testing
Invitae RCV000496538 SCV000635140 likely benign Hereditary breast and ovarian cancer syndrome 2017-02-09 criteria provided, single submitter clinical testing

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