ClinVar Miner

List of variants in gene ZEB2 reported as likely benign by GeneDx

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Gene type:
ClinVar version:
Total variants: 107
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HGVS dbSNP
NM_014795.3(ZEB2):c.404-11dup rs770071448
NM_014795.3(ZEB2):c.74-20_74-19delGT rs1491378666
NM_014795.4(ZEB2):c.*6T>G rs1057522759
NM_014795.4(ZEB2):c.-18T>G rs764963313
NM_014795.4(ZEB2):c.-38C>G rs730881182
NM_014795.4(ZEB2):c.-52C>T rs1261328970
NM_014795.4(ZEB2):c.-64G>A rs1057522589
NM_014795.4(ZEB2):c.-70+8T>C rs1057521945
NM_014795.4(ZEB2):c.1008T>C (p.Gly336=)
NM_014795.4(ZEB2):c.1048A>G (p.Thr350Ala) rs730881175
NM_014795.4(ZEB2):c.1050G>A (p.Thr350=)
NM_014795.4(ZEB2):c.10C>G (p.Pro4Ala) rs146394306
NM_014795.4(ZEB2):c.1233C>T (p.Gly411=) rs1057522114
NM_014795.4(ZEB2):c.1264G>A (p.Ala422Thr) rs141793065
NM_014795.4(ZEB2):c.1276T>A (p.Leu426Ile) rs201881288
NM_014795.4(ZEB2):c.1288C>T (p.Pro430Ser) rs753804606
NM_014795.4(ZEB2):c.1306A>G (p.Met436Val) rs145812868
NM_014795.4(ZEB2):c.1322T>G (p.Val441Gly) rs775301918
NM_014795.4(ZEB2):c.1336C>T (p.Pro446Ser) rs1435380197
NM_014795.4(ZEB2):c.139G>T (p.Ala47Ser) rs730881184
NM_014795.4(ZEB2):c.141T>A (p.Ala47=) rs1250280865
NM_014795.4(ZEB2):c.1526C>T (p.Pro509Leu) rs1051563603
NM_014795.4(ZEB2):c.1527G>A (p.Pro509=) rs759999662
NM_014795.4(ZEB2):c.1534G>A (p.Gly512Ser) rs141781307
NM_014795.4(ZEB2):c.1542G>A (p.Pro514=) rs141674976
NM_014795.4(ZEB2):c.158C>A (p.Ala53Asp) rs730881185
NM_014795.4(ZEB2):c.1638C>T (p.Asp546=) rs149035844
NM_014795.4(ZEB2):c.1678C>T (p.Arg560Cys) rs730881194
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.1839C>G (p.Val613=) rs751367896
NM_014795.4(ZEB2):c.1880T>G (p.Val627Gly) rs730881176
NM_014795.4(ZEB2):c.1945A>C (p.Ile649Leu) rs730881177
NM_014795.4(ZEB2):c.1949A>C (p.Asn650Thr) rs1057520817
NM_014795.4(ZEB2):c.1953A>G (p.Pro651=) rs779951735
NM_014795.4(ZEB2):c.2004G>T (p.Glu668Asp) rs767506087
NM_014795.4(ZEB2):c.2016T>C (p.Asp672=) rs1057522531
NM_014795.4(ZEB2):c.2084G>A (p.Arg695Gln) rs147693839
NM_014795.4(ZEB2):c.2120C>T (p.Ser707Phe) rs1174325176
NM_014795.4(ZEB2):c.2205_2206delinsCG (p.Met736Val) rs1060500654
NM_014795.4(ZEB2):c.2206A>G (p.Met736Val) rs139191491
NM_014795.4(ZEB2):c.2215A>G (p.Ile739Val) rs730881178
NM_014795.4(ZEB2):c.2226A>T (p.Pro742=) rs540345773
NM_014795.4(ZEB2):c.222G>A (p.Val74=) rs767831638
NM_014795.4(ZEB2):c.2255C>G (p.Thr752Arg) rs143438888
NM_014795.4(ZEB2):c.2255C>T (p.Thr752Met) rs143438888
NM_014795.4(ZEB2):c.2256G>A (p.Thr752=) rs772121083
NM_014795.4(ZEB2):c.225C>T (p.Ser75=) rs754754722
NM_014795.4(ZEB2):c.2300C>T (p.Thr767Ile) rs755233964
NM_014795.4(ZEB2):c.2352T>C (p.Ser784=) rs201990887
NM_014795.4(ZEB2):c.2457A>G (p.Ser819=) rs144184948
NM_014795.4(ZEB2):c.2495C>A (p.Ala832Asp) rs730881179
NM_014795.4(ZEB2):c.257A>G (p.Asp86Gly)
NM_014795.4(ZEB2):c.2622T>A (p.Asn874Lys) rs745927130
NM_014795.4(ZEB2):c.2627A>G (p.Asp876Gly)
NM_014795.4(ZEB2):c.2646A>G (p.Pro882=) rs372224804
NM_014795.4(ZEB2):c.2733A>G (p.Pro911=)
NM_014795.4(ZEB2):c.2746A>G (p.Ser916Gly) rs1057520707
NM_014795.4(ZEB2):c.2855G>C (p.Arg952Thr) rs151256895
NM_014795.4(ZEB2):c.2870G>A (p.Arg957Gln) rs371509136
NM_014795.4(ZEB2):c.2886+12A>C rs1057524071
NM_014795.4(ZEB2):c.2886+4A>C rs754532627
NM_014795.4(ZEB2):c.2887-7A>C rs1553961365
NM_014795.4(ZEB2):c.2907A>G (p.Ala969=) rs1057521876
NM_014795.4(ZEB2):c.295A>G (p.Asn99Asp) rs150665982
NM_014795.4(ZEB2):c.297C>T (p.Asn99=) rs147603619
NM_014795.4(ZEB2):c.304A>T (p.Ile102Phe) rs201109457
NM_014795.4(ZEB2):c.3057C>T (p.Tyr1019=) rs541915540
NM_014795.4(ZEB2):c.314C>A (p.Ala105Asp) rs730881207
NM_014795.4(ZEB2):c.314C>T (p.Ala105Val) rs730881207
NM_014795.4(ZEB2):c.3153C>T (p.Gly1051=) rs1057522295
NM_014795.4(ZEB2):c.3201G>A (p.Ser1067=) rs730881180
NM_014795.4(ZEB2):c.3219C>T (p.His1073=) rs139944383
NM_014795.4(ZEB2):c.3286C>A (p.Arg1096Ser)
NM_014795.4(ZEB2):c.3337T>A (p.Leu1113Met) rs730881204
NM_014795.4(ZEB2):c.3353C>A (p.Pro1118His) rs780004720
NM_014795.4(ZEB2):c.3432C>T (p.Gly1144=) rs768007761
NM_014795.4(ZEB2):c.3452T>C (p.Leu1151Pro) rs1553960747
NM_014795.4(ZEB2):c.349T>C (p.Tyr117His) rs1057522108
NM_014795.4(ZEB2):c.3513T>C (p.Ser1171=) rs1553960736
NM_014795.4(ZEB2):c.3557G>T (p.Gly1186Val) rs748213160
NM_014795.4(ZEB2):c.3563A>G (p.His1188Arg) rs730881181
NM_014795.4(ZEB2):c.3582G>A (p.Ser1194=) rs1057522691
NM_014795.4(ZEB2):c.3640A>G (p.Met1214Val) rs199951665
NM_014795.4(ZEB2):c.374C>T (p.Thr125Met) rs727504227
NM_014795.4(ZEB2):c.384C>T (p.Thr128=) rs573552493
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.396T>C (p.Asn132=) rs147072510
NM_014795.4(ZEB2):c.403+19G>A
NM_014795.4(ZEB2):c.593-240C>A
NM_014795.4(ZEB2):c.621T>C (p.Phe207=) rs934470843
NM_014795.4(ZEB2):c.702C>T (p.His234=) rs140169964
NM_014795.4(ZEB2):c.720C>T (p.Asn240=) rs1022840384
NM_014795.4(ZEB2):c.73+113G>T
NM_014795.4(ZEB2):c.73+217C>G
NM_014795.4(ZEB2):c.73+6A>C rs756924190
NM_014795.4(ZEB2):c.730C>T (p.Pro244Ser) rs730881190
NM_014795.4(ZEB2):c.74-15G>T rs908922006
NM_014795.4(ZEB2):c.756C>T (p.Tyr252=) rs1553962059
NM_014795.4(ZEB2):c.773G>A (p.Arg258Gln) rs730881173
NM_014795.4(ZEB2):c.797G>A (p.Gly266Glu) rs1057522361
NM_014795.4(ZEB2):c.798G>A (p.Gly266=) rs34961586
NM_014795.4(ZEB2):c.828A>G (p.Gly276=) rs1161704021
NM_014795.4(ZEB2):c.89A>G (p.Asn30Ser) rs1057522155
NM_014795.4(ZEB2):c.981G>A (p.Ser327=) rs201579452
NM_014795.4(ZEB2):c.9G>A (p.Gln3=) rs149882004

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