ClinVar Miner

Submissions for variant NM_004304.5(ALK):c.3520T>C (p.Phe1174Leu) (rs281864719)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Database of Curated Mutations (DoCM) RCV000421904 SCV000510427 likely pathogenic Neuroblastoma 2016-05-13 no assertion criteria provided literature only
Division of Genomic Diagnostics,The Children's Hospital of Philadelphia RCV000201883 SCV000256813 pathogenic Neuroblastoma 3 2015-10-07 no assertion criteria provided clinical testing

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