ClinVar Miner

List of variants in gene DGUOK reported as uncertain significance for not provided

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Total variants: 78
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HGVS dbSNP gnomAD frequency
NM_080916.3(DGUOK):c.509A>G (p.Gln170Arg) rs74874677 0.01472
NM_080916.3(DGUOK):c.630G>A (p.Glu210=) rs115206553 0.00075
NM_080916.3(DGUOK):c.708-3T>C rs370071744 0.00061
NM_080916.3(DGUOK):c.211C>G (p.Pro71Ala) rs184770596 0.00044
NM_080916.3(DGUOK):c.256-7C>T rs199531052 0.00031
NM_080916.3(DGUOK):c.199G>A (p.Val67Ile) rs62641679 0.00029
NM_080916.3(DGUOK):c.664C>T (p.Leu222=) rs375686551 0.00023
NM_080916.3(DGUOK):c.462T>A (p.Asn154Lys) rs144181978 0.00021
NM_080916.3(DGUOK):c.366G>C (p.Gln122His) rs199645258 0.00016
NM_080916.3(DGUOK):c.-1G>A rs754623273 0.00010
NM_080916.3(DGUOK):c.758A>G (p.Asn253Ser) rs200169027 0.00006
NM_080916.3(DGUOK):c.649G>A (p.Ala217Thr) rs577526451 0.00005
NM_080916.3(DGUOK):c.697A>G (p.Lys233Glu) rs371342464 0.00005
NM_080916.3(DGUOK):c.547C>T (p.Arg183Trp) rs373204746 0.00004
NM_080916.3(DGUOK):c.792A>C (p.Glu264Asp) rs745732447 0.00004
NM_080916.3(DGUOK):c.444-11C>G rs536746349 0.00003
NM_080916.3(DGUOK):c.653A>G (p.Tyr218Cys) rs137902450 0.00003
NM_080916.3(DGUOK):c.206C>T (p.Thr69Ile) rs560564448 0.00002
NM_080916.3(DGUOK):c.256-6C>T rs568816337 0.00002
NM_080916.3(DGUOK):c.280A>G (p.Asn94Asp) rs747937764 0.00002
NM_080916.3(DGUOK):c.302G>A (p.Arg101Gln) rs1250828551 0.00002
NM_080916.3(DGUOK):c.314G>A (p.Arg105Gln) rs776244110 0.00002
NM_080916.3(DGUOK):c.337T>C (p.Phe113Leu) rs141810774 0.00002
NM_080916.3(DGUOK):c.143-4G>A rs544350167 0.00001
NM_080916.3(DGUOK):c.265G>A (p.Ala89Thr) rs138683121 0.00001
NM_080916.3(DGUOK):c.301C>T (p.Arg101Trp) rs770571614 0.00001
NM_080916.3(DGUOK):c.370G>A (p.Glu124Lys) rs777559041 0.00001
NM_080916.3(DGUOK):c.405G>A (p.Lys135=) rs775871024 0.00001
NM_080916.3(DGUOK):c.808-10C>G rs758503693 0.00001
NM_080916.2(DGUOK):c.707+3_707+6dupAAGT
NM_080916.3(DGUOK):c.-5G>T
NM_080916.3(DGUOK):c.143-10T>G
NM_080916.3(DGUOK):c.143-6T>C
NM_080916.3(DGUOK):c.152A>G (p.Lys51Arg) rs1064794680
NM_080916.3(DGUOK):c.158C>A (p.Thr53Lys)
NM_080916.3(DGUOK):c.176C>G (p.Thr59Arg) rs144907403
NM_080916.3(DGUOK):c.176C>T (p.Thr59Met) rs144907403
NM_080916.3(DGUOK):c.197A>T (p.His66Leu)
NM_080916.3(DGUOK):c.198C>A (p.His66Gln) rs138034585
NM_080916.3(DGUOK):c.218C>G (p.Ala73Gly)
NM_080916.3(DGUOK):c.256-3T>C
NM_080916.3(DGUOK):c.257C>A (p.Ala86Asp)
NM_080916.3(DGUOK):c.275T>A (p.Leu92His) rs982717858
NM_080916.3(DGUOK):c.290A>G (p.Asp97Gly)
NM_080916.3(DGUOK):c.297G>A (p.Met99Ile)
NM_080916.3(DGUOK):c.319T>C (p.Ser107Pro) rs2104944559
NM_080916.3(DGUOK):c.343T>C (p.Phe115Leu)
NM_080916.3(DGUOK):c.361G>C (p.Val121Leu) rs756158114
NM_080916.3(DGUOK):c.388C>T (p.Leu130Phe)
NM_080916.3(DGUOK):c.394C>G (p.Gln132Glu)
NM_080916.3(DGUOK):c.436A>G (p.Ser146Gly)
NM_080916.3(DGUOK):c.444-75TC[9] rs140339626
NM_080916.3(DGUOK):c.450C>G (p.Ile150Met)
NM_080916.3(DGUOK):c.463C>A (p.Leu155Ile)
NM_080916.3(DGUOK):c.466T>C (p.Phe156Leu)
NM_080916.3(DGUOK):c.545G>C (p.Ser182Thr)
NM_080916.3(DGUOK):c.549G>T (p.Arg183=) rs1558661806
NM_080916.3(DGUOK):c.559C>T (p.His187Tyr) rs1558661819
NM_080916.3(DGUOK):c.566T>C (p.Phe189Ser)
NM_080916.3(DGUOK):c.574C>T (p.Leu192Phe)
NM_080916.3(DGUOK):c.584C>T (p.Ser195Phe)
NM_080916.3(DGUOK):c.592G>T (p.Val198Phe) rs1428988311
NM_080916.3(DGUOK):c.596G>C (p.Cys199Ser)
NM_080916.3(DGUOK):c.601A>G (p.Lys201Glu) rs1558668852
NM_080916.3(DGUOK):c.604A>G (p.Arg202Gly)
NM_080916.3(DGUOK):c.663G>T (p.Gln221His) rs957798169
NM_080916.3(DGUOK):c.688C>T (p.Leu230Phe) rs1347001625
NM_080916.3(DGUOK):c.700A>C (p.Thr234Pro)
NM_080916.3(DGUOK):c.704C>G (p.Thr235Arg) rs375774789
NM_080916.3(DGUOK):c.704C>T (p.Thr235Met) rs375774789
NM_080916.3(DGUOK):c.707A>G (p.Lys236Arg) rs2105001965
NM_080916.3(DGUOK):c.736C>T (p.Pro246Ser)
NM_080916.3(DGUOK):c.737C>G (p.Pro246Arg)
NM_080916.3(DGUOK):c.772G>A (p.Glu258Lys) rs868377068
NM_080916.3(DGUOK):c.787_789del (p.Gln263del)
NM_080916.3(DGUOK):c.796C>T (p.Leu266Phe)
NM_080916.3(DGUOK):c.814A>G (p.Thr272Ala)
NM_080916.3(DGUOK):c.827A>C (p.Asn276Thr)

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