ClinVar Miner

List of variants in gene CDK4 reported as likely benign for Hereditary cancer-predisposing syndrome

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 54
Download table as spreadsheet
HGVS dbSNP
NM_000075.4(CDK4):c.122A>G (p.Asn41Ser) rs144890720
NM_000075.4(CDK4):c.12T>C (p.Ser4=) rs1595111261
NM_000075.4(CDK4):c.141A>C (p.Gly47=) rs863224320
NM_000075.4(CDK4):c.147T>C (p.Leu49=) rs1060504383
NM_000075.4(CDK4):c.153C>T (p.Ile51=) rs1555201373
NM_000075.4(CDK4):c.165T>G (p.Arg55=) rs1595111002
NM_000075.4(CDK4):c.168G>A (p.Glu56=) rs1555201371
NM_000075.4(CDK4):c.180G>A (p.Leu60=) rs1555201367
NM_000075.4(CDK4):c.183G>A (p.Arg61=) rs771902016
NM_000075.4(CDK4):c.210T>C (p.Asn70=) rs1162061851
NM_000075.4(CDK4):c.222G>A (p.Leu74=) rs565645344
NM_000075.4(CDK4):c.228C>T (p.Asp76=) rs772531745
NM_000075.4(CDK4):c.252C>T (p.Asp84=) rs780590939
NM_000075.4(CDK4):c.258G>A (p.Glu86=) rs1247612368
NM_000075.4(CDK4):c.279T>C (p.Phe93=) rs1478574297
NM_000075.4(CDK4):c.285T>C (p.His95=) rs757492324
NM_000075.4(CDK4):c.297C>T (p.Asp99=) rs1595110736
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.324C>G (p.Pro108=) rs774075369
NM_000075.4(CDK4):c.334T>C (p.Leu112=) rs1555201318
NM_000075.4(CDK4):c.342C>T (p.Ala114=) rs762471901
NM_000075.4(CDK4):c.348G>A (p.Thr116=) rs761353033
NM_000075.4(CDK4):c.381C>T (p.Gly127=) rs781207390
NM_000075.4(CDK4):c.402T>C (p.Asn134=) rs537039467
NM_000075.4(CDK4):c.408C>A (p.Ile136=) rs758331285
NM_000075.4(CDK4):c.408C>T (p.Ile136=) rs758331285
NM_000075.4(CDK4):c.420T>C (p.Asp140=) rs863224321
NM_000075.4(CDK4):c.423G>A (p.Leu141=) rs760242081
NM_000075.4(CDK4):c.42C>T (p.Val14=) rs786203182
NM_000075.4(CDK4):c.444G>T (p.Val148=) rs1595110484
NM_000075.4(CDK4):c.459A>G (p.Thr153=) rs1595110466
NM_000075.4(CDK4):c.481C>T (p.Leu161=) rs796860515
NM_000075.4(CDK4):c.486C>G (p.Ala162=) rs1595110441
NM_000075.4(CDK4):c.501C>T (p.Tyr167=) rs1316207187
NM_000075.4(CDK4):c.513T>C (p.Leu171=) rs748319770
NM_000075.4(CDK4):c.519C>T (p.Pro173=) rs747084709
NM_000075.4(CDK4):c.522+8G>A rs758294834
NM_000075.4(CDK4):c.534C>G (p.Leu178=) rs11547327
NM_000075.4(CDK4):c.534C>T (p.Leu178=) rs11547327
NM_000075.4(CDK4):c.549C>T (p.Pro183=) rs778696237
NM_000075.4(CDK4):c.561G>T (p.Leu187=) rs864622342
NM_000075.4(CDK4):c.567C>T (p.Ser189=) rs144422354
NM_000075.4(CDK4):c.573T>C (p.Tyr191=) rs878853623
NM_000075.4(CDK4):c.576A>C (p.Ala192=) rs565563672
NM_000075.4(CDK4):c.597T>C (p.Ser199=) rs1260582581
NM_000075.4(CDK4):c.60G>A (p.Val20=) rs1595111186
NM_000075.4(CDK4):c.612T>C (p.Phe204=) rs1555201266
NM_000075.4(CDK4):c.625C>T (p.Arg209Cys) rs140644696
NM_000075.4(CDK4):c.632+434A>G rs869312546
NM_000075.4(CDK4):c.84T>C (p.Ser28=) rs763203404
NM_000075.4(CDK4):c.87C>G (p.Gly29=) rs1555201376
NM_000075.4(CDK4):c.96G>C (p.Val32=) rs563392051

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.