ClinVar Miner

Submissions for variant NM_000059.4(BRCA2):c.781G>C (p.Ala261Pro)

dbSNP: rs1135401831
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Total submissions: 1
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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 RCV000496918 SCV000586919 uncertain significance Hereditary breast ovarian cancer syndrome 2016-04-14 no assertion criteria provided clinical testing

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