ClinVar Miner

Submissions for variant NM_000075.4(CDK4):c.210T>C (p.Asn70=) (rs1162061851)

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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV000975296 SCV001123179 likely benign not provided 2018-10-08 criteria provided, single submitter clinical testing
Ambry Genetics RCV001014465 SCV001175175 likely benign Hereditary cancer-predisposing syndrome 2019-02-14 criteria provided, single submitter clinical testing Synonymous alterations with insufficient evidence to classify as benign
Invitae RCV001397181 SCV001598926 likely benign Hereditary melanoma 2018-10-06 criteria provided, single submitter clinical testing

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