ClinVar Miner

List of variants in gene CDK4 reported as likely benign for not specified

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Gene type:
ClinVar version:
Total variants: 23
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HGVS dbSNP
NM_000075.4(CDK4):c.-11T>C rs746754426
NM_000075.4(CDK4):c.-32G>T rs1371795570
NM_000075.4(CDK4):c.-9G>T rs779962297
NM_000075.4(CDK4):c.180G>A (p.Leu60=) rs1555201367
NM_000075.4(CDK4):c.222G>A (p.Leu74=) rs565645344
NM_000075.4(CDK4):c.261C>A (p.Ile87=) rs779482890
NM_000075.4(CDK4):c.288A>G (p.Val96=) rs754092304
NM_000075.4(CDK4):c.306A>C (p.Thr102=) rs201202764
NM_000075.4(CDK4):c.306A>G (p.Thr102=) rs201202764
NM_000075.4(CDK4):c.309T>C (p.Tyr103=) rs554603181
NM_000075.4(CDK4):c.342C>G (p.Ala114=) rs762471901
NM_000075.4(CDK4):c.355-12C>T rs1004281478
NM_000075.4(CDK4):c.420T>C (p.Asp140=) rs863224321
NM_000075.4(CDK4):c.423G>C (p.Leu141=) rs760242081
NM_000075.4(CDK4):c.481C>T (p.Leu161=) rs796860515
NM_000075.4(CDK4):c.519C>T (p.Pro173=) rs747084709
NM_000075.4(CDK4):c.522+18A>G rs1555201289
NM_000075.4(CDK4):c.549C>T (p.Pro183=) rs778696237
NM_000075.4(CDK4):c.564G>A (p.Gln188=) rs1057521685
NM_000075.4(CDK4):c.625C>T (p.Arg209Cys) rs140644696
NM_000075.4(CDK4):c.6T>A (p.Ala2=) rs1057523632
NM_000075.4(CDK4):c.78C>T (p.Pro26=) rs1057523487
NM_000075.4(CDK4):c.84T>C (p.Ser28=) rs763203404

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