ClinVar Miner

Submissions for variant NM_000075.4(CDK4):c.198T>C (p.Phe66=)

dbSNP: rs1595110954
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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 RCV000895508 SCV001039553 likely benign Familial melanoma 2024-10-21 criteria provided, single submitter clinical testing
Myriad Genetics, Inc. RCV004792575 SCV005405069 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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