ClinVar Miner

Submissions for variant NM_058216.3(RAD51C):c.420A>G (p.Val140=) (rs1060504672)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV000471281 SCV000560784 likely benign not provided 2016-11-24 criteria provided, single submitter clinical testing
Ambry Genetics RCV000572119 SCV000667137 likely benign Hereditary cancer-predisposing syndrome 2017-06-14 criteria provided, single submitter clinical testing Lines of evidence used in support of classification: Synonymous alterations with insufficient evidence to classify as benign

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