ClinVar Miner

Submissions for variant NM_000075.4(CDK4):c.786T>C (p.Pro262=)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV003086175 SCV003472904 likely benign Familial melanoma 2024-09-09 criteria provided, single submitter clinical testing
Myriad Genetics, Inc. RCV004790364 SCV005405042 benign Melanoma, cutaneous malignant, susceptibility to, 3 2024-09-26 criteria provided, single submitter clinical testing This variant is considered benign. This variant is a silent/synonymous amino acid change and it is not expected to impact splicing.

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