ClinVar Miner

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

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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Database of Curated Mutations (DoCM) RCV000442440 SCV000505151 likely pathogenic Lung adenocarcinoma 2014-12-26 no assertion criteria provided literature only
Database of Curated Mutations (DoCM) RCV000427324 SCV000505152 likely pathogenic Neuroblastoma 2016-05-31 no assertion criteria provided literature only
Division of Genomic Diagnostics,The Children's Hospital of Philadelphia RCV000201904 SCV000256817 pathogenic Neuroblastoma 3 2015-11-06 no assertion criteria provided clinical testing

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