ClinVar Miner

Submissions for variant NM_000075.4(CDK4):c.632+9C>T

gnomAD frequency: 0.00001  dbSNP: rs1192976748
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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 RCV000559216 SCV000637380 likely benign Familial melanoma 2024-05-21 criteria provided, single submitter clinical testing
Mendelics RCV000709230 SCV000838661 uncertain significance Melanoma, cutaneous malignant, susceptibility to, 3 2018-07-02 criteria provided, single submitter clinical testing
Myriad Genetics, Inc. RCV000709230 SCV005405408 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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