ClinVar Miner

Submissions for variant NM_053056.3(CCND1):c.735G>A (p.Arg245=)

gnomAD frequency: 0.00042  dbSNP: rs201299704
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV000912402 SCV001057507 benign not provided 2018-07-10 criteria provided, single submitter clinical testing
CeGaT Center for Human Genetics Tuebingen RCV000912402 SCV004137125 likely benign not provided 2022-09-01 criteria provided, single submitter clinical testing CCND1: BP4, BP7
Breakthrough Genomics, Breakthrough Genomics RCV000912402 SCV005321529 benign not provided criteria provided, single submitter not provided

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