ClinVar Miner

Submissions for variant NM_000075.4(CDK4):c.71G>T (p.Arg24Leu) (rs104894340)

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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) RCV000431833 SCV000505857 likely pathogenic Lung adenocarcinoma 2016-05-31 no assertion criteria provided literature only
Database of Curated Mutations (DoCM) RCV000442117 SCV000505858 likely pathogenic Multiple myeloma 2016-05-31 no assertion criteria provided literature only
Database of Curated Mutations (DoCM) RCV000427015 SCV000505859 likely pathogenic Malignant melanoma of skin 2016-05-31 no assertion criteria provided literature only

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