ClinVar Miner

List of variants in gene DUOX2 studied for not specified

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Gene type:
ClinVar version:
Total variants: 79
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HGVS dbSNP gnomAD frequency
NM_001363711.2(DUOX2):c.3515+15T>A rs269869 0.99253
NM_001363711.2(DUOX2):c.413C>T (p.Pro138Leu) rs2001616 0.75375
NM_001363711.2(DUOX2):c.3200C>T (p.Ser1067Leu) rs269868 0.71631
NM_001363711.2(DUOX2):c.2033A>G (p.His678Arg) rs57659670 0.17189
NM_001363711.2(DUOX2):c.2334+10C>T rs73406330 0.09464
NM_001363711.2(DUOX2):c.4479C>G (p.Pro1493=) rs56323146 0.08342
NM_001363711.2(DUOX2):c.2148+9C>T rs73406337 0.07581
NM_001363711.2(DUOX2):c.2286G>A (p.Gln762=) rs73406334 0.07466
NM_001363711.2(DUOX2):c.2102G>A (p.Arg701Gln) rs113400262 0.04972
NM_001363711.2(DUOX2):c.3050A>G (p.Glu1017Gly) rs79393107 0.03767
NM_001363711.2(DUOX2):c.3966C>T (p.Ser1322=) rs61730032 0.02613
NM_001363711.2(DUOX2):c.1693+10G>A rs76411432 0.02317
NM_001363711.2(DUOX2):c.908C>G (p.Pro303Arg) rs151261408 0.01090
NM_001363711.2(DUOX2):c.1921G>A (p.Glu641Lys) rs139161034 0.00343
NM_001363711.2(DUOX2):c.2544G>C (p.Leu848=) rs139095108 0.00232
NM_001363711.2(DUOX2):c.597G>C (p.Ser199=) rs2467828 0.00148
NM_001363711.2(DUOX2):c.598G>A (p.Gly200Arg) rs2467827 0.00142
NM_001363711.2(DUOX2):c.3232G>A (p.Val1078Met) rs147772932 0.00125
NM_001363711.2(DUOX2):c.303C>A (p.Arg101=) rs117041393 0.00124
NM_001363711.2(DUOX2):c.3155G>A (p.Cys1052Tyr) rs76343591 0.00109
NM_001363711.2(DUOX2):c.567C>T (p.His189=) rs2467829 0.00078
NM_001363711.2(DUOX2):c.1709A>T (p.Gln570Leu) rs547116063 0.00042
NM_001363711.2(DUOX2):c.3103G>A (p.Val1035Met) rs138774384 0.00041
NM_001363711.2(DUOX2):c.1547G>A (p.Arg516His) rs143818717 0.00026
NM_001363711.2(DUOX2):c.2335-3C>T rs369394906 0.00017
NM_001363711.2(DUOX2):c.4049C>T (p.Pro1350Leu) rs140035596 0.00017
NM_001363711.2(DUOX2):c.1060C>T (p.Arg354Trp) rs766496010 0.00014
NM_001363711.2(DUOX2):c.1189C>A (p.Gln397Lys) rs200989933 0.00009
NM_001363711.2(DUOX2):c.883-13C>G rs368847158 0.00008
NM_001363711.2(DUOX2):c.2504G>A (p.Gly835Asp) rs772637424 0.00006
NM_001363711.2(DUOX2):c.1546C>T (p.Arg516Cys) rs138461488 0.00004
NM_001363711.2(DUOX2):c.4036A>G (p.Ile1346Val) rs149848729 0.00004
NM_001363711.2(DUOX2):c.4240-18C>T rs755550994 0.00004
NM_001363711.2(DUOX2):c.3239T>C (p.Ile1080Thr) rs756822740 0.00002
NM_001363711.2(DUOX2):c.3260C>T (p.Ala1087Val) rs776772769 0.00002
NM_001363711.2(DUOX2):c.3416-14T>C rs369781783 0.00002
NM_001363711.2(DUOX2):c.3689C>T (p.Ala1230Val) rs557220354 0.00002
NM_001363711.2(DUOX2):c.841C>T (p.Leu281=) rs1481616548 0.00002
NM_001363711.2(DUOX2):c.1087A>G (p.Ser363Gly) rs1311288291 0.00001
NM_001363711.2(DUOX2):c.144C>A (p.His48Gln) rs779289206 0.00001
NM_001363711.2(DUOX2):c.1718A>G (p.Gln573Arg) rs748027232 0.00001
NM_001363711.2(DUOX2):c.214G>T (p.Ala72Ser) rs199733766 0.00001
NM_001363711.2(DUOX2):c.2803C>T (p.Leu935Phe) rs767244088 0.00001
NM_001363711.2(DUOX2):c.2935G>A (p.Gly979Arg) rs1291549758 0.00001
NM_001363711.2(DUOX2):c.3116G>A (p.Arg1039Gln) rs772992566 0.00001
NM_001363711.2(DUOX2):c.3382C>T (p.Arg1128Cys) rs559663716 0.00001
NM_001363711.2(DUOX2):c.3521A>G (p.Lys1174Arg) rs775017655 0.00001
NM_001363711.2(DUOX2):c.3940G>A (p.Glu1314Lys) rs759698581 0.00001
NM_001363711.2(DUOX2):c.4261C>T (p.Arg1421Trp) rs775445309 0.00001
NM_001363711.2(DUOX2):c.4575T>C (p.Asn1525=) rs145877502 0.00001
NM_001363711.2(DUOX2):c.4631A>G (p.His1544Arg) rs754342496 0.00001
NM_001363711.2(DUOX2):c.838G>A (p.Glu280Lys) rs912581499 0.00001
NM_001363711.2(DUOX2):c.1001A>T (p.Gln334Leu) rs1461096460
NM_001363711.2(DUOX2):c.1315C>G (p.Pro439Ala) rs781544455
NM_001363711.2(DUOX2):c.1461G>C (p.Gly487=) rs269860
NM_001363711.2(DUOX2):c.1587G>T (p.Lys529Asn) rs746483045
NM_001363711.2(DUOX2):c.199G>A (p.Asp67Asn) rs1255757517
NM_001363711.2(DUOX2):c.272G>A (p.Gly91Asp)
NM_001363711.2(DUOX2):c.2779A>T (p.Met927Leu)
NM_001363711.2(DUOX2):c.2793_2796delinsCAAT (p.Asp932Asn) rs1064796650
NM_001363711.2(DUOX2):c.2944C>G (p.Pro982Ala) rs61730030
NM_001363711.2(DUOX2):c.3267C>G (p.Ser1089Arg) rs202085990
NM_001363711.2(DUOX2):c.3395T>A (p.Met1132Lys) rs189585637
NM_001363711.2(DUOX2):c.3416-13C>T rs1555412892
NM_001363711.2(DUOX2):c.355G>C (p.Val119Leu) rs138970496
NM_001363711.2(DUOX2):c.3607T>C (p.Tyr1203His)
NM_001363711.2(DUOX2):c.3656G>C (p.Trp1219Ser)
NM_001363711.2(DUOX2):c.3721A>T (p.Ile1241Phe) rs1422217875
NM_001363711.2(DUOX2):c.3830C>G (p.Ala1277Gly) rs143471358
NM_001363711.2(DUOX2):c.4080G>T (p.Lys1360Asn) rs374891282
NM_001363711.2(DUOX2):c.4244A>G (p.Tyr1415Cys)
NM_001363711.2(DUOX2):c.4408C>A (p.Arg1470=) rs200785525
NM_001363711.2(DUOX2):c.4469T>A (p.Phe1490Tyr)
NM_001363711.2(DUOX2):c.4478C>G (p.Pro1493Arg)
NM_001363711.2(DUOX2):c.4541T>C (p.Val1514Ala)
NM_001363711.2(DUOX2):c.4552G>C (p.Gly1518Arg)
NM_001363711.2(DUOX2):c.528G>C (p.Thr176=)
NM_001363711.2(DUOX2):c.587_619del (p.Arg196_Gly206del) rs1894402738
NM_001363711.2(DUOX2):c.597_598delinsCA (p.Gly200Arg)

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