ClinVar Miner

Submissions for variant NM_000051.3(ATM):c.3558A>T (p.Glu1186Asp) (rs12786957)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Ambry Genetics RCV000572499 SCV000672682 uncertain significance Hereditary cancer-predisposing syndrome 2016-11-02 criteria provided, single submitter clinical testing Lines of evidence used in support of classification: Insufficient evidence,In silico models in agreement (benign)

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