ClinVar Miner

Submissions for variant NM_000075.4(CDK4):c.48C>T (p.Ala16=)

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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 RCV002637123 SCV003512436 likely benign Familial melanoma 2024-12-31 criteria provided, single submitter clinical testing
Center for Genomic Medicine, Rigshospitalet, Copenhagen University Hospital RCV003493981 SCV004243474 likely benign not specified 2024-02-06 criteria provided, single submitter clinical testing
Myriad Genetics, Inc. RCV004786844 SCV005404475 benign Melanoma, cutaneous malignant, susceptibility to, 3 2024-09-24 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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