ClinVar Miner

Submissions for variant NM_032043.2(BRIP1):c.1659A>G (p.Gln553=) (rs876660693)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Ambry Genetics RCV000222322 SCV000278326 likely benign Hereditary cancer-predisposing syndrome 2015-09-13 criteria provided, single submitter clinical testing Synonymous alterations with insufficient evidence to classify as benign;In silico models in agreement (benign)
Integrated Genetics/Laboratory Corporation of America RCV000781180 SCV000919062 likely benign not specified 2019-08-28 criteria provided, single submitter clinical testing

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