ClinVar Miner

Submissions for variant NM_004304.5(ALK):c.3586C>A (p.Leu1196Met)

dbSNP: rs1057519784
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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) RCV000424376 SCV000505149 likely pathogenic Lung adenocarcinoma 2014-12-26 no assertion criteria provided literature only
Database of Curated Mutations (DoCM) RCV000435601 SCV000505150 not provided Non-small cell lung carcinoma 2016-03-10 no assertion provided literature only
Molekularpathologisches Zentrum, Universitaetsklinikum Heidelberg RCV002282133 SCV002571105 likely pathogenic Lung cancer no assertion criteria provided clinical testing

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