ClinVar Miner

Submissions for variant NM_000075.4(CDK4):c.70C>A (p.Arg24Ser)

dbSNP: rs11547328
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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) RCV000437447 SCV000505863 likely pathogenic Lung adenocarcinoma 2016-05-31 no assertion criteria provided literature only
Database of Curated Mutations (DoCM) RCV000419745 SCV000505864 likely pathogenic Malignant melanoma of skin 2016-05-31 no assertion criteria provided literature only
Database of Curated Mutations (DoCM) RCV000429137 SCV000505865 likely pathogenic Multiple myeloma 2016-05-31 no assertion criteria provided literature only

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