ClinVar Miner

Submissions for variant NM_000075.4(CDK4):c.684-14C>T

gnomAD frequency: 0.00001  dbSNP: rs750471090
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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 RCV002126035 SCV002452827 likely benign Familial melanoma 2024-11-28 criteria provided, single submitter clinical testing
Myriad Genetics, Inc. RCV004785514 SCV005407009 likely benign Melanoma, cutaneous malignant, susceptibility to, 3 2024-09-26 criteria provided, single submitter clinical testing This variant is considered likely benign. This variant is intronic and is not expected to impact mRNA splicing.

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