ClinVar Miner

List of variants in gene ZEB2 reported as uncertain significance for Mowat-Wilson syndrome

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Gene type:
ClinVar version:
Total variants: 128
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HGVS dbSNP
NM_014795.4(ZEB2):c.*1110_*1114AAGAG[1] rs534438826
NM_014795.4(ZEB2):c.*116G>A rs886054896
NM_014795.4(ZEB2):c.*1256G>A rs765985290
NM_014795.4(ZEB2):c.*1405C>A rs886054893
NM_014795.4(ZEB2):c.*1637C>G rs886054892
NM_014795.4(ZEB2):c.*1704A>G rs761671531
NM_014795.4(ZEB2):c.*1770G>A rs886054891
NM_014795.4(ZEB2):c.*1796dup rs886054890
NM_014795.4(ZEB2):c.*1839A>G rs886054889
NM_014795.4(ZEB2):c.*1918A>C rs768430700
NM_014795.4(ZEB2):c.*1945del rs886054888
NM_014795.4(ZEB2):c.*1984del rs771457697
NM_014795.4(ZEB2):c.*1985A>T rs886054887
NM_014795.4(ZEB2):c.*1992T>C rs558354594
NM_014795.4(ZEB2):c.*2060C>A rs886054886
NM_014795.4(ZEB2):c.*2181T>C rs886054885
NM_014795.4(ZEB2):c.*2377_*2378GT[7] rs886054884
NM_014795.4(ZEB2):c.*2388_*2389TA[10] rs143648355
NM_014795.4(ZEB2):c.*2388_*2389TA[11] rs143648355
NM_014795.4(ZEB2):c.*2388_*2389TA[12] rs143648355
NM_014795.4(ZEB2):c.*2388_*2389TA[8] rs143648355
NM_014795.4(ZEB2):c.*2396_*2397insGT rs886054883
NM_014795.4(ZEB2):c.*2525dup rs886054882
NM_014795.4(ZEB2):c.*2532G>C rs558500049
NM_014795.4(ZEB2):c.*2554T>C rs886054881
NM_014795.4(ZEB2):c.*2948G>T rs111991965
NM_014795.4(ZEB2):c.*2966T>C rs886054880
NM_014795.4(ZEB2):c.*3010C>T rs886054879
NM_014795.4(ZEB2):c.*3025A>G rs886054878
NM_014795.4(ZEB2):c.*3194C>T rs867937417
NM_014795.4(ZEB2):c.*3357C>G rs886054877
NM_014795.4(ZEB2):c.*3444G>A rs751537725
NM_014795.4(ZEB2):c.*3955A>G rs886054876
NM_014795.4(ZEB2):c.*4250G>A rs886054875
NM_014795.4(ZEB2):c.*4305A>G rs886054874
NM_014795.4(ZEB2):c.*4603T>C rs757098887
NM_014795.4(ZEB2):c.*4844_*4845dup rs201661554
NM_014795.4(ZEB2):c.*4845dup rs201661554
NM_014795.4(ZEB2):c.*4848C>A rs886054873
NM_014795.4(ZEB2):c.*4942A>G rs886054872
NM_014795.4(ZEB2):c.*496A>G rs886054895
NM_014795.4(ZEB2):c.*514del rs558553086
NM_014795.4(ZEB2):c.*514dup rs558553086
NM_014795.4(ZEB2):c.*560del rs533637050
NM_014795.4(ZEB2):c.*560dup rs533637050
NM_014795.4(ZEB2):c.-205T>C rs886054898
NM_014795.4(ZEB2):c.10C>G (p.Pro4Ala) rs146394306
NM_014795.4(ZEB2):c.1113C>T (p.Asn371=) rs886054897
NM_014795.4(ZEB2):c.1222G>A (p.Gly408Arg)
NM_014795.4(ZEB2):c.1276T>A (p.Leu426Ile) rs201881288
NM_014795.4(ZEB2):c.1283T>C (p.Val428Ala) rs730881192
NM_014795.4(ZEB2):c.1288C>T (p.Pro430Ser) rs753804606
NM_014795.4(ZEB2):c.1309C>A (p.Gln437Lys) rs760437173
NM_014795.4(ZEB2):c.139G>T (p.Ala47Ser) rs730881184
NM_014795.4(ZEB2):c.1410T>C (p.Thr470=) rs34890427
NM_014795.4(ZEB2):c.1426A>C (p.Met476Leu) rs778246270
NM_014795.4(ZEB2):c.1491A>C (p.Gln497His) rs200378546
NM_014795.4(ZEB2):c.1565C>G (p.Thr522Ser) rs730881193
NM_014795.4(ZEB2):c.1571G>A (p.Ser524Asn) rs1560606972
NM_014795.4(ZEB2):c.1735A>G (p.Thr579Ala) rs140593583
NM_014795.4(ZEB2):c.179C>T (p.Thr60Met) rs780890592
NM_014795.4(ZEB2):c.1845G>T (p.Gln615His)
NM_014795.4(ZEB2):c.1876G>A (p.Gly626Arg) rs727504224
NM_014795.4(ZEB2):c.1877G>A (p.Gly626Glu) rs794727923
NM_014795.4(ZEB2):c.1880T>A (p.Val627Asp) rs730881176
NM_014795.4(ZEB2):c.1975C>T (p.Leu659Phe) rs1560606673
NM_014795.4(ZEB2):c.1993A>G (p.Met665Val) rs1388932284
NM_014795.4(ZEB2):c.2084G>A (p.Arg695Gln) rs147693839
NM_014795.4(ZEB2):c.2226A>T (p.Pro742=) rs540345773
NM_014795.4(ZEB2):c.2239C>T (p.Leu747Phe)
NM_014795.4(ZEB2):c.2248A>G (p.Ser750Gly) rs730881196
NM_014795.4(ZEB2):c.2255C>T (p.Thr752Met) rs143438888
NM_014795.4(ZEB2):c.2327A>G (p.Asp776Gly) rs1553961558
NM_014795.4(ZEB2):c.2329C>T (p.His777Tyr) rs587784564
NM_014795.4(ZEB2):c.2337G>C (p.Arg779Ser)
NM_014795.4(ZEB2):c.2352T>C (p.Ser784=) rs201990887
NM_014795.4(ZEB2):c.2354C>G (p.Pro785Arg) rs1560606278
NM_014795.4(ZEB2):c.2390A>G (p.His797Arg)
NM_014795.4(ZEB2):c.2418C>A (p.Phe806Leu)
NM_014795.4(ZEB2):c.2471T>C (p.Met824Thr) rs1553961536
NM_014795.4(ZEB2):c.2497A>G (p.Thr833Ala) rs1490526407
NM_014795.4(ZEB2):c.2541C>A (p.Asn847Lys)
NM_014795.4(ZEB2):c.2545G>A (p.Val849Ile) rs1560606101
NM_014795.4(ZEB2):c.2621A>C (p.Asn874Thr) rs1477010525
NM_014795.4(ZEB2):c.2622T>A (p.Asn874Lys) rs745927130
NM_014795.4(ZEB2):c.2641A>C (p.Asn881His) rs794727922
NM_014795.4(ZEB2):c.2647G>A (p.Val883Met)
NM_014795.4(ZEB2):c.2692C>T (p.Leu898Phe)
NM_014795.4(ZEB2):c.2762G>A (p.Arg921Gln) rs147716561
NM_014795.4(ZEB2):c.2774G>A (p.Gly925Glu) rs1408659659
NM_014795.4(ZEB2):c.2855G>C (p.Arg952Thr) rs151256895
NM_014795.4(ZEB2):c.2869C>T (p.Arg957Trp) rs1354236085
NM_014795.4(ZEB2):c.2870G>A (p.Arg957Gln) rs371509136
NM_014795.4(ZEB2):c.2886+4_2886+5del rs1560605795
NM_014795.4(ZEB2):c.2951C>T (p.Ser984Phe) rs143474223
NM_014795.4(ZEB2):c.295_297AAC[1] (p.Asn100del) rs587776610
NM_014795.4(ZEB2):c.3070A>G (p.Lys1024Glu)
NM_014795.4(ZEB2):c.3141G>C (p.Arg1047Ser) rs587784567
NM_014795.4(ZEB2):c.3202_3207del (p.Gly1068_Ser1069del) rs1553960777
NM_014795.4(ZEB2):c.3267A>C (p.Glu1089Asp) rs1553960775
NM_014795.4(ZEB2):c.3298C>T (p.His1100Tyr)
NM_014795.4(ZEB2):c.3308C>A (p.Pro1103His)
NM_014795.4(ZEB2):c.332-6C>T rs730881186
NM_014795.4(ZEB2):c.3327C>A (p.Asn1109Lys) rs1288140327
NM_014795.4(ZEB2):c.3357G>C (p.Gln1119His) rs1332911302
NM_014795.4(ZEB2):c.3408C>G (p.Ser1136Arg) rs1060500655
NM_014795.4(ZEB2):c.3444C>T (p.Tyr1148=) rs374141392
NM_014795.4(ZEB2):c.3451C>A (p.Leu1151Met) rs772764893
NM_014795.4(ZEB2):c.3536T>C (p.Ile1179Thr) rs1238900874
NM_014795.4(ZEB2):c.3538C>G (p.Arg1180Gly)
NM_014795.4(ZEB2):c.3575A>C (p.Asp1192Ala) rs752093966
NM_014795.4(ZEB2):c.3599A>G (p.Glu1200Gly) rs1273805127
NM_014795.4(ZEB2):c.3640A>G (p.Met1214Val) rs199951665
NM_014795.4(ZEB2):c.364C>T (p.Pro122Ser)
NM_014795.4(ZEB2):c.385G>A (p.Ala129Thr) rs730881187
NM_014795.4(ZEB2):c.395A>G (p.Asn132Ser) rs369622877
NM_014795.4(ZEB2):c.430T>A (p.Phe144Ile) rs1057518371
NM_014795.4(ZEB2):c.466C>T (p.Arg156Cys) rs147021269
NM_014795.4(ZEB2):c.467G>A (p.Arg156His) rs1250217464
NM_014795.4(ZEB2):c.59C>T (p.Pro20Leu)
NM_014795.4(ZEB2):c.703G>A (p.Glu235Lys) rs1553962069
NM_014795.4(ZEB2):c.73+6A>C rs756924190
NM_014795.4(ZEB2):c.747G>A (p.Thr249=) rs587784569
NM_014795.4(ZEB2):c.751G>A (p.Ala251Thr)
NM_014795.4(ZEB2):c.797G>A (p.Gly266Glu) rs1057522361
NM_014795.4(ZEB2):c.82_87del (p.Tyr28_Asp29del) rs730881214
NM_014795.4(ZEB2):c.933G>T (p.Glu311Asp)
NM_014795.4(ZEB2):c.9G>A (p.Gln3=) rs149882004

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