ClinVar Miner

Submissions for variant NM_004304.5(ALK):c.3600G>A (p.Ala1200=) (rs56247462)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV000233243 SCV000288349 benign Neuroblastoma 3 2018-01-02 criteria provided, single submitter clinical testing
Ambry Genetics RCV000561311 SCV000672468 likely benign Hereditary cancer-predisposing syndrome 2016-12-14 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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