ClinVar Miner

List of variants in gene CDK4 reported as uncertain significance for not specified

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Total variants: 20
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HGVS dbSNP gnomAD frequency
NM_000075.4(CDK4):c.625C>T (p.Arg209Cys) rs140644696 0.00029
NM_000075.4(CDK4):c.254G>A (p.Arg85Gln) rs587778184 0.00003
NM_000075.4(CDK4):c.-2G>A rs771607042 0.00001
NM_000075.4(CDK4):c.219-7T>C rs543798269 0.00001
NM_000075.4(CDK4):c.245G>A (p.Arg82Gln) rs3211612 0.00001
NM_000075.4(CDK4):c.346A>G (p.Thr116Ala) rs2063052002 0.00001
NM_000075.4(CDK4):c.352A>C (p.Lys118Gln) rs772689692 0.00001
NM_000075.4(CDK4):c.365G>A (p.Arg122His) rs34386532 0.00001
NM_000075.4(CDK4):c.523G>A (p.Val175Ile) rs587778186 0.00001
NM_000075.4(CDK4):c.553G>A (p.Val185Ile) rs757302656 0.00001
NM_000075.4(CDK4):c.605G>C (p.Cys202Ser) rs1424791303 0.00001
NM_000075.4(CDK4):c.629G>A (p.Arg210Gln) rs373619077 0.00001
NM_000075.4(CDK4):c.262A>C (p.Lys88Gln) rs2140387459
NM_000075.4(CDK4):c.310C>A (p.Leu104Met) rs759535768
NM_000075.4(CDK4):c.369G>T (p.Gln123His) rs1955231243
NM_000075.4(CDK4):c.376A>G (p.Arg126Gly) rs1565806573
NM_000075.4(CDK4):c.479G>T (p.Gly160Val)
NM_000075.4(CDK4):c.590T>C (p.Met197Thr) rs975342748
NM_000075.4(CDK4):c.632+5dup rs1555201260
NM_000075.4(CDK4):c.632A>C (p.Lys211Thr) rs765656720

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