ClinVar Miner

Submissions for variant NM_000075.4(CDK4):c.261C>T (p.Ile87=) (rs779482890)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV000463189 SCV000559059 likely benign not provided 2016-08-10 criteria provided, single submitter clinical testing
Invitae RCV001459034 SCV001662867 likely benign Hereditary melanoma 2016-08-08 criteria provided, single submitter clinical testing

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