ClinVar Miner

Submissions for variant NM_004304.5(ALK):c.3604G>A (p.Gly1202Arg)

dbSNP: rs1057519783
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Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Baylor Genetics RCV004567902 SCV005059710 uncertain significance Neuroblastoma, susceptibility to, 3 2023-12-19 criteria provided, single submitter clinical testing
Database of Curated Mutations (DoCM) RCV000432713 SCV000505147 likely pathogenic Lung adenocarcinoma 2014-12-26 no assertion criteria provided literature only
Database of Curated Mutations (DoCM) RCV000443402 SCV000505148 not provided Non-small cell lung carcinoma 2016-03-10 no assertion provided literature only
Molekularpathologisches Zentrum, Universitaetsklinikum Heidelberg RCV002282132 SCV002571107 likely pathogenic Lung cancer no assertion criteria provided clinical testing

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