ClinVar Miner

Submissions for variant NM_004304.5(ALK):c.3522C>A (p.Phe1174Leu) (rs863225281)

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Total submissions: 5
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Database of Curated Mutations (DoCM) RCV000444781 SCV000503776 pathogenic Neuroblastoma 2016-03-10 no assertion criteria provided literature only
Database of Curated Mutations (DoCM) RCV000426846 SCV000503777 likely pathogenic Lung adenocarcinoma 2014-12-26 no assertion criteria provided literature only
Database of Curated Mutations (DoCM) RCV000435780 SCV000503778 not provided Benign Soft Tissue Neoplasm of Uncertain Differentiation 2016-03-10 no assertion provided literature only
Database of Curated Mutations (DoCM) RCV000418576 SCV000503779 not provided Non-small cell lung cancer 2016-03-10 no assertion provided literature only
Division of Genomic Diagnostics,The Children's Hospital of Philadelphia RCV000201882 SCV000256816 pathogenic Neuroblastoma 3 2015-10-07 no assertion criteria provided clinical testing

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