ClinVar Miner

Submissions for variant NM_000075.4(CDK4):c.420T>C (p.Asp140=) (rs863224321)

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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV000195600 SCV000253069 likely benign Hereditary melanoma 2020-04-12 criteria provided, single submitter clinical testing
Ambry Genetics RCV000566913 SCV000669103 likely benign Hereditary cancer-predisposing syndrome 2017-04-11 criteria provided, single submitter clinical testing Synonymous alterations with insufficient evidence to classify as benign
Women's Health and Genetics/Laboratory Corporation of America, LabCorp RCV001193396 SCV001362181 likely benign not specified 2019-10-26 criteria provided, single submitter clinical testing

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