ClinVar Miner

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

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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 RCV000572499 SCV000672682 uncertain significance Hereditary cancer-predisposing syndrome 2016-11-02 criteria provided, single submitter clinical testing Insufficient evidence;In silico models in agreement (benign)
Color RCV000572499 SCV001354052 uncertain significance Hereditary cancer-predisposing syndrome 2019-06-05 criteria provided, single submitter clinical testing

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