ClinVar Miner

Submissions for variant NM_004304.5(ALK):c.3806G>C (p.Gly1269Ala) (rs1057519781)

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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) RCV000423107 SCV000505143 likely pathogenic Lung adenocarcinoma 2014-12-26 no assertion criteria provided literature only
Database of Curated Mutations (DoCM) RCV000432491 SCV000505144 not provided Non-small cell lung cancer 2016-03-10 no assertion provided literature only

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