ClinVar Miner

List of variants in gene CDK4 reported as uncertain significance for Hereditary cancer-predisposing syndrome

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Total variants: 161
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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.460G>C (p.Val154Leu) rs563692823 0.00004
NM_000075.4(CDK4):c.254G>A (p.Arg85Gln) rs587778184 0.00003
NM_000075.4(CDK4):c.354+3G>C rs746395249 0.00003
NM_000075.4(CDK4):c.409G>A (p.Val137Ile) rs150281463 0.00003
NM_000075.4(CDK4):c.542G>A (p.Arg181Gln) rs772079285 0.00003
NM_000075.4(CDK4):c.364C>T (p.Arg122Cys) rs587778185 0.00002
NM_000075.4(CDK4):c.451G>A (p.Gly151Ser) rs1280774592 0.00002
NM_000075.4(CDK4):c.-2G>A rs771607042 0.00001
NM_000075.4(CDK4):c.109G>A (p.Val37Met) rs1060501930 0.00001
NM_000075.4(CDK4):c.14G>A (p.Arg5Gln) rs1031329993 0.00001
NM_000075.4(CDK4):c.219-5G>C rs1286893141 0.00001
NM_000075.4(CDK4):c.229G>A (p.Val77Ile) rs730881670 0.00001
NM_000075.4(CDK4):c.245G>A (p.Arg82Gln) rs3211612 0.00001
NM_000075.4(CDK4):c.263A>G (p.Lys88Arg) rs1463751654 0.00001
NM_000075.4(CDK4):c.343G>A (p.Glu115Lys) rs772938517 0.00001
NM_000075.4(CDK4):c.347C>T (p.Thr116Met) rs1060501931 0.00001
NM_000075.4(CDK4):c.349A>G (p.Ile117Val) rs776343973 0.00001
NM_000075.4(CDK4):c.352A>C (p.Lys118Gln) rs772689692 0.00001
NM_000075.4(CDK4):c.355-4C>G rs1406247863 0.00001
NM_000075.4(CDK4):c.364C>G (p.Arg122Gly) rs587778185 0.00001
NM_000075.4(CDK4):c.385G>A (p.Asp129Asn) rs876660606 0.00001
NM_000075.4(CDK4):c.404G>A (p.Cys135Tyr) rs1340574386 0.00001
NM_000075.4(CDK4):c.415C>T (p.Arg139Ter) rs753579957 0.00001
NM_000075.4(CDK4):c.416G>A (p.Arg139Gln) rs763652580 0.00001
NM_000075.4(CDK4):c.421C>G (p.Leu141Val) rs1246306482 0.00001
NM_000075.4(CDK4):c.431A>G (p.Glu144Gly) rs863224603 0.00001
NM_000075.4(CDK4):c.458C>T (p.Thr153Ile) rs1443076952 0.00001
NM_000075.4(CDK4):c.461T>C (p.Val154Ala) rs1555201304 0.00001
NM_000075.4(CDK4):c.491T>C (p.Ile164Thr) rs1222529576 0.00001
NM_000075.4(CDK4):c.520G>A (p.Val174Met) rs780052789 0.00001
NM_000075.4(CDK4):c.522+1G>A rs1281910320 0.00001
NM_000075.4(CDK4):c.523G>A (p.Val175Ile) rs587778186 0.00001
NM_000075.4(CDK4):c.532C>T (p.Leu178Phe) rs1030964946 0.00001
NM_000075.4(CDK4):c.553G>A (p.Val185Ile) rs757302656 0.00001
NM_000075.4(CDK4):c.580C>T (p.Pro194Ser) rs1264069202 0.00001
NM_000075.4(CDK4):c.605G>C (p.Cys202Ser) rs1424791303 0.00001
NM_000075.4(CDK4):c.626G>A (p.Arg209His) rs754423955 0.00001
NM_000075.4(CDK4):c.629G>A (p.Arg210Gln) rs373619077 0.00001
NM_000075.4(CDK4):c.-4G>C
NM_000075.4(CDK4):c.-5T>C
NM_000075.4(CDK4):c.104A>T (p.Lys35Met)
NM_000075.4(CDK4):c.107G>A (p.Ser36Asn)
NM_000075.4(CDK4):c.118C>T (p.Pro40Ser)
NM_000075.4(CDK4):c.11C>T (p.Ser4Phe)
NM_000075.4(CDK4):c.13C>G (p.Arg5Gly) rs1595111256
NM_000075.4(CDK4):c.17_18del (p.Arg5_Tyr6insTer)
NM_000075.4(CDK4):c.19G>A (p.Glu7Lys) rs1000052939
NM_000075.4(CDK4):c.219-3C>A
NM_000075.4(CDK4):c.219G>C (p.Arg73=)
NM_000075.4(CDK4):c.221T>C (p.Leu74Pro)
NM_000075.4(CDK4):c.223A>G (p.Met75Val) rs1343218987
NM_000075.4(CDK4):c.223_230dup (p.Cys78fs) rs2140387576
NM_000075.4(CDK4):c.225G>A (p.Met75Ile) rs1595110823
NM_000075.4(CDK4):c.228C>A (p.Asp76Glu)
NM_000075.4(CDK4):c.233G>C (p.Cys78Ser) rs1595110816
NM_000075.4(CDK4):c.235G>A (p.Ala79Thr) rs1555201333
NM_000075.4(CDK4):c.239C>T (p.Thr80Ile)
NM_000075.4(CDK4):c.244C>G (p.Arg82Gly) rs1398120196
NM_000075.4(CDK4):c.253C>G (p.Arg85Gly) rs759017803
NM_000075.4(CDK4):c.260T>G (p.Ile87Ser) rs1555201326
NM_000075.4(CDK4):c.265G>A (p.Val89Ile) rs1190779336
NM_000075.4(CDK4):c.269C>T (p.Thr90Ile) rs1955234447
NM_000075.4(CDK4):c.287T>C (p.Val96Ala) rs1955234241
NM_000075.4(CDK4):c.289G>C (p.Asp97His) rs1060501932
NM_000075.4(CDK4):c.291C>A (p.Asp97Glu) rs1595110740
NM_000075.4(CDK4):c.304A>G (p.Thr102Ala)
NM_000075.4(CDK4):c.310C>A (p.Leu104Met) rs759535768
NM_000075.4(CDK4):c.313G>C (p.Asp105His)
NM_000075.4(CDK4):c.315C>G (p.Asp105Glu) rs1158206003
NM_000075.4(CDK4):c.316A>C (p.Lys106Gln) rs1595110711
NM_000075.4(CDK4):c.323C>A (p.Pro108His) rs1595110706
NM_000075.4(CDK4):c.325C>G (p.Pro109Ala)
NM_000075.4(CDK4):c.326C>T (p.Pro109Leu) rs1595110701
NM_000075.4(CDK4):c.328C>T (p.Pro110Ser)
NM_000075.4(CDK4):c.329C>T (p.Pro110Leu)
NM_000075.4(CDK4):c.32A>C (p.Glu11Ala)
NM_000075.4(CDK4):c.331G>A (p.Gly111Ser) rs1277385976
NM_000075.4(CDK4):c.332G>A (p.Gly111Asp)
NM_000075.4(CDK4):c.336G>T (p.Leu112Phe) rs1595110684
NM_000075.4(CDK4):c.338C>A (p.Pro113Gln) rs1955233297
NM_000075.4(CDK4):c.343G>C (p.Glu115Gln) rs772938517
NM_000075.4(CDK4):c.353A>G (p.Lys118Arg) rs1555201314
NM_000075.4(CDK4):c.354+3G>A rs746395249
NM_000075.4(CDK4):c.354+3G>T
NM_000075.4(CDK4):c.354+5G>T
NM_000075.4(CDK4):c.355G>C (p.Asp119His) rs2140386821
NM_000075.4(CDK4):c.358C>A (p.Leu120Met)
NM_000075.4(CDK4):c.374T>C (p.Leu125Pro)
NM_000075.4(CDK4):c.380G>A (p.Gly127Asp)
NM_000075.4(CDK4):c.397G>A (p.Ala133Thr) rs751684879
NM_000075.4(CDK4):c.401A>G (p.Asn134Ser) rs1595110530
NM_000075.4(CDK4):c.409G>C (p.Val137Leu) rs150281463
NM_000075.4(CDK4):c.415C>G (p.Arg139Gly) rs753579957
NM_000075.4(CDK4):c.418G>C (p.Asp140His) rs1555201308
NM_000075.4(CDK4):c.418G>T (p.Asp140Tyr) rs1555201308
NM_000075.4(CDK4):c.426G>T (p.Lys142Asn)
NM_000075.4(CDK4):c.428C>T (p.Pro143Leu)
NM_000075.4(CDK4):c.42del (p.Gly15fs)
NM_000075.4(CDK4):c.434A>G (p.Asn145Ser)
NM_000075.4(CDK4):c.43G>A (p.Gly15Ser) rs1355460580
NM_000075.4(CDK4):c.440T>C (p.Leu147Pro)
NM_000075.4(CDK4):c.442G>C (p.Val148Leu) rs1595110489
NM_000075.4(CDK4):c.452G>A (p.Gly151Asp) rs1595110472
NM_000075.4(CDK4):c.455del (p.Gly152fs)
NM_000075.4(CDK4):c.458C>A (p.Thr153Lys)
NM_000075.4(CDK4):c.469G>T (p.Ala157Ser)
NM_000075.4(CDK4):c.470C>G (p.Ala157Gly)
NM_000075.4(CDK4):c.477del (p.Phe159fs) rs786203016
NM_000075.4(CDK4):c.484G>T (p.Ala162Ser) rs1555201301
NM_000075.4(CDK4):c.489A>T (p.Arg163Ser) rs876658462
NM_000075.4(CDK4):c.48C>G (p.Ala16=) rs1311074831
NM_000075.4(CDK4):c.493T>G (p.Tyr165Asp)
NM_000075.4(CDK4):c.496A>G (p.Ser166Gly) rs1487656600
NM_000075.4(CDK4):c.497G>C (p.Ser166Thr) rs876660536
NM_000075.4(CDK4):c.49T>C (p.Tyr17His) rs1555201383
NM_000075.4(CDK4):c.500A>G (p.Tyr167Cys)
NM_000075.4(CDK4):c.502C>G (p.Gln168Glu)
NM_000075.4(CDK4):c.502C>T (p.Gln168Ter) rs1555201299
NM_000075.4(CDK4):c.504G>C (p.Gln168His) rs770086242
NM_000075.4(CDK4):c.515C>T (p.Thr172Ile)
NM_000075.4(CDK4):c.517C>A (p.Pro173Thr) rs768904034
NM_000075.4(CDK4):c.522+4A>G rs1595110395
NM_000075.4(CDK4):c.529A>G (p.Thr177Ala) rs1555201280
NM_000075.4(CDK4):c.529dup (p.Thr177fs)
NM_000075.4(CDK4):c.537G>T (p.Trp179Cys)
NM_000075.4(CDK4):c.541C>G (p.Arg181Gly) rs1595110257
NM_000075.4(CDK4):c.541C>T (p.Arg181Ter)
NM_000075.4(CDK4):c.549_567del (p.Glu184fs) rs1955226726
NM_000075.4(CDK4):c.550G>A (p.Glu184Lys) rs1595110227
NM_000075.4(CDK4):c.55A>G (p.Thr19Ala) rs1595111197
NM_000075.4(CDK4):c.562C>A (p.Gln188Lys) rs1555201274
NM_000075.4(CDK4):c.56C>G (p.Thr19Arg)
NM_000075.4(CDK4):c.56C>T (p.Thr19Ile)
NM_000075.4(CDK4):c.571T>A (p.Tyr191Asn) rs1955226614
NM_000075.4(CDK4):c.572A>G (p.Tyr191Cys) rs1955226587
NM_000075.4(CDK4):c.575C>G (p.Ala192Gly) rs2140385751
NM_000075.4(CDK4):c.577A>G (p.Thr193Ala)
NM_000075.4(CDK4):c.577A>T (p.Thr193Ser) rs543769986
NM_000075.4(CDK4):c.581C>T (p.Pro194Leu) rs1198423952
NM_000075.4(CDK4):c.583G>A (p.Val195Met) rs1955226317
NM_000075.4(CDK4):c.590T>C (p.Met197Thr) rs975342748
NM_000075.4(CDK4):c.595A>C (p.Ser199Arg)
NM_000075.4(CDK4):c.599T>C (p.Val200Ala) rs1060501929
NM_000075.4(CDK4):c.5C>T (p.Ala2Val)
NM_000075.4(CDK4):c.602G>T (p.Gly201Val)
NM_000075.4(CDK4):c.610T>A (p.Phe204Ile) rs1955226021
NM_000075.4(CDK4):c.613G>A (p.Ala205Thr) rs368013594
NM_000075.4(CDK4):c.623T>C (p.Phe208Ser)
NM_000075.4(CDK4):c.629G>C (p.Arg210Pro) rs373619077
NM_000075.4(CDK4):c.632+4T>A rs1397979744
NM_000075.4(CDK4):c.632+5G>A
NM_000075.4(CDK4):c.632A>C (p.Lys211Thr) rs765656720
NM_000075.4(CDK4):c.632A>T (p.Lys211Met) rs765656720
NM_000075.4(CDK4):c.63C>T (p.Tyr21=)
NM_000075.4(CDK4):c.64A>C (p.Lys22Gln) rs1555201381
NM_000075.4(CDK4):c.67G>T (p.Ala23Ser)
NM_000075.4(CDK4):c.85G>A (p.Gly29Ser)
NM_000075.4(CDK4):c.88C>T (p.His30Tyr) rs750707985
NM_000075.4(CDK4):c.93T>G (p.Phe31Leu) rs1595111145
NM_000075.4(CDK4):c.98C>T (p.Ala33Val)

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