ClinVar Miner

Submissions for variant NM_000075.4(CDK4):c.820-6C>T

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Myriad Genetics, Inc. RCV004791942 SCV005405084 likely benign Melanoma, cutaneous malignant, susceptibility to, 3 2024-09-27 criteria provided, single submitter clinical testing This variant is considered likely benign. This variant is intronic and is not expected to impact mRNA splicing.
Labcorp Genetics (formerly Invitae), Labcorp RCV005061432 SCV005705786 likely benign Familial melanoma 2025-01-14 criteria provided, single submitter clinical testing

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