ClinVar Miner

List of variants in gene DUOX2 reported by PreventionGenetics, part of Exact Sciences

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Gene type:
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Total variants: 60
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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.2286G>A (p.Gln762=) rs73406334 0.07585
NM_001363711.2(DUOX2):c.2148+9C>T rs73406337 0.07581
NM_001363711.2(DUOX2):c.2102G>A (p.Arg701Gln) rs113400262 0.04972
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.3261G>A (p.Ala1087=) rs79480907 0.01330
NM_001363711.2(DUOX2):c.908C>G (p.Pro303Arg) rs151261408 0.01090
NM_001363711.2(DUOX2):c.2182G>A (p.Ala728Thr) rs138353181 0.00700
NM_001363711.2(DUOX2):c.3856T>C (p.Tyr1286His) rs148968706 0.00452
NM_001363711.2(DUOX2):c.1921G>A (p.Glu641Lys) rs139161034 0.00343
NM_001363711.2(DUOX2):c.3081G>A (p.Lys1027=) rs78876145 0.00338
NM_001363711.2(DUOX2):c.3759G>A (p.Pro1253=) rs140663764 0.00307
NM_001363711.2(DUOX2):c.2704G>A (p.Glu902Lys) rs138926644 0.00179
NM_001363711.2(DUOX2):c.1621C>A (p.Arg541=) rs140940946 0.00096
NM_001363711.2(DUOX2):c.3055A>G (p.Met1019Val) rs148053632 0.00086
NM_001363711.2(DUOX2):c.243G>A (p.Pro81=) rs369158930 0.00056
NM_001363711.2(DUOX2):c.2906G>A (p.Arg969Gln) rs146664125 0.00056
NM_001363711.2(DUOX2):c.3185-9C>T rs148813922 0.00051
NM_001363711.2(DUOX2):c.1462G>A (p.Gly488Arg) rs191759494 0.00024
NM_001363711.2(DUOX2):c.1196C>T (p.Ser399Leu) rs147435713 0.00020
NM_001363711.2(DUOX2):c.1126C>T (p.Arg376Trp) rs119472029 0.00014
NM_001363711.2(DUOX2):c.3789G>A (p.Val1263=) rs369176278 0.00011
NM_001363711.2(DUOX2):c.4552G>A (p.Gly1518Ser) rs368512412 0.00008
NM_001363711.2(DUOX2):c.2297G>A (p.Arg766His) rs545643570 0.00005
NM_001363711.2(DUOX2):c.1295G>A (p.Arg432His) rs530736554 0.00004
NM_001363711.2(DUOX2):c.192T>C (p.Asn64=) rs112584857 0.00004
NM_001363711.2(DUOX2):c.3627C>T (p.His1209=) rs145751273 0.00002
NM_001363711.2(DUOX2):c.4561G>T (p.Gly1521Ter) rs765781255 0.00001
NM_001363711.2(DUOX2):c.1040+1G>T
NM_001363711.2(DUOX2):c.1131+8T>A rs370387994
NM_001363711.2(DUOX2):c.1335G>C (p.Leu445=)
NM_001363711.2(DUOX2):c.1461G>C (p.Gly487=) rs269860
NM_001363711.2(DUOX2):c.1461G>T (p.Gly487=) rs269860
NM_001363711.2(DUOX2):c.1977C>T (p.Ser659=)
NM_001363711.2(DUOX2):c.261A>C (p.Ala87=)
NM_001363711.2(DUOX2):c.2654G>T (p.Arg885Leu) rs181461079
NM_001363711.2(DUOX2):c.2713G>T (p.Glu905Ter)
NM_001363711.2(DUOX2):c.2757G>C (p.Leu919=)
NM_001363711.2(DUOX2):c.2794_2796delinsAAT (p.Asp932Asn)
NM_001363711.2(DUOX2):c.2894C>T (p.Ser965Leu)
NM_001363711.2(DUOX2):c.2895_2898del (p.Phe966fs) rs530719719
NM_001363711.2(DUOX2):c.2944C>G (p.Pro982Ala) rs61730030
NM_001363711.2(DUOX2):c.3006-15_3006-3del
NM_001363711.2(DUOX2):c.3076C>T (p.Gln1026Ter)
NM_001363711.2(DUOX2):c.3288T>C (p.Tyr1096=)
NM_001363711.2(DUOX2):c.3819C>T (p.Ser1273=) rs750148604
NM_001363711.2(DUOX2):c.3830C>G (p.Ala1277Gly) rs143471358
NM_001363711.2(DUOX2):c.3847+9C>T
NM_001363711.2(DUOX2):c.4239+3G>T
NM_001363711.2(DUOX2):c.4240-5C>T
NM_001363711.2(DUOX2):c.4623C>T (p.Phe1541=)
NM_001363711.2(DUOX2):c.602dup (p.Gln202fs) rs567500345
NM_001363711.2(DUOX2):c.618dup (p.Pro207fs)
NM_001363711.2(DUOX2):c.715G>C (p.Ala239Pro)

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