ClinVar Miner

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

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 80
Download table as spreadsheet
HGVS dbSNP
NM_014795.4(ZEB2):c.1008T>C (p.Gly336=) rs149510351
NM_014795.4(ZEB2):c.1053T>C (p.Gly351=) rs1553961766
NM_014795.4(ZEB2):c.1071T>G (p.Val357=) rs200510665
NM_014795.4(ZEB2):c.1221C>T (p.His407=) rs144613207
NM_014795.4(ZEB2):c.1240C>A (p.Pro414Thr) rs755425183
NM_014795.4(ZEB2):c.1276T>A (p.Leu426Ile) rs201881288
NM_014795.4(ZEB2):c.1306A>G (p.Met436Val) rs145812868
NM_014795.4(ZEB2):c.1315T>C (p.Leu439=) rs1060503991
NM_014795.4(ZEB2):c.1353C>T (p.Pro451=) rs1573717237
NM_014795.4(ZEB2):c.1386G>C (p.Lys462Asn) rs780523431
NM_014795.4(ZEB2):c.1387G>A (p.Val463Ile)
NM_014795.4(ZEB2):c.1438G>T (p.Ala480Ser) rs143854197
NM_014795.4(ZEB2):c.1470C>T (p.His490=) rs767360787
NM_014795.4(ZEB2):c.1476G>A (p.Lys492=) rs368316666
NM_014795.4(ZEB2):c.1480C>T (p.Pro494Ser) rs144952836
NM_014795.4(ZEB2):c.1503A>G (p.Gln501=) rs1269576350
NM_014795.4(ZEB2):c.1527G>A (p.Pro509=) rs759999662
NM_014795.4(ZEB2):c.1542G>T (p.Pro514=) rs141674976
NM_014795.4(ZEB2):c.1638C>T (p.Asp546=) rs149035844
NM_014795.4(ZEB2):c.168G>C (p.Leu56=) rs1553964156
NM_014795.4(ZEB2):c.1735A>G (p.Thr579Ala) rs140593583
NM_014795.4(ZEB2):c.1737T>A (p.Thr579=) rs1573716677
NM_014795.4(ZEB2):c.180G>A (p.Thr60=) rs372888487
NM_014795.4(ZEB2):c.1836G>A (p.Ala612=) rs754916469
NM_014795.4(ZEB2):c.1845G>T (p.Gln615His) rs757485792
NM_014795.4(ZEB2):c.1848T>G (p.Pro616=) rs144835963
NM_014795.4(ZEB2):c.1876G>A (p.Gly626Arg) rs727504224
NM_014795.4(ZEB2):c.1880T>A (p.Val627Asp) rs730881176
NM_014795.4(ZEB2):c.1890T>C (p.Asp630=) rs1220461554
NM_014795.4(ZEB2):c.1965C>T (p.His655=) rs1290881093
NM_014795.4(ZEB2):c.2016T>C (p.Asp672=) rs1057522531
NM_014795.4(ZEB2):c.2085A>G (p.Arg695=) rs1573716167
NM_014795.4(ZEB2):c.2120C>T (p.Ser707Phe) rs1174325176
NM_014795.4(ZEB2):c.216A>C (p.Pro72=) rs764560219
NM_014795.4(ZEB2):c.2175C>T (p.Asp725=) rs1184693387
NM_014795.4(ZEB2):c.219C>T (p.His73=) rs778851716
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.2255C>T (p.Thr752Met) rs143438888
NM_014795.4(ZEB2):c.225C>T (p.Ser75=) rs754754722
NM_014795.4(ZEB2):c.2325G>A (p.Leu775=) rs1553961560
NM_014795.4(ZEB2):c.2342A>G (p.Asn781Ser) rs750936389
NM_014795.4(ZEB2):c.2352T>C (p.Ser784=) rs201990887
NM_014795.4(ZEB2):c.2373A>G (p.Thr791=) rs775082191
NM_014795.4(ZEB2):c.2374T>C (p.Ser792Pro)
NM_014795.4(ZEB2):c.2385C>T (p.Asn795=) rs759505392
NM_014795.4(ZEB2):c.2457A>G (p.Ser819=) rs144184948
NM_014795.4(ZEB2):c.2541C>T (p.Asn847=) rs759097498
NM_014795.4(ZEB2):c.2547T>C (p.Val849=) rs908943407
NM_014795.4(ZEB2):c.2646A>G (p.Pro882=) rs372224804
NM_014795.4(ZEB2):c.2647G>A (p.Val883Met) rs550047043
NM_014795.4(ZEB2):c.2762G>A (p.Arg921Gln) rs147716561
NM_014795.4(ZEB2):c.2766A>T (p.Pro922=) rs185223937
NM_014795.4(ZEB2):c.2808C>T (p.Ala936=) rs749708858
NM_014795.4(ZEB2):c.2824G>A (p.Gly942Arg)
NM_014795.4(ZEB2):c.2886+4_2886+5del rs1560605795
NM_014795.4(ZEB2):c.2997T>C (p.Tyr999=) rs1573713486
NM_014795.4(ZEB2):c.3067+8T>A rs1573713416
NM_014795.4(ZEB2):c.30C>T (p.Pro10=) rs747483109
NM_014795.4(ZEB2):c.3219C>T (p.His1073=) rs139944383
NM_014795.4(ZEB2):c.324T>C (p.Asp108=) rs148117680
NM_014795.4(ZEB2):c.3295G>C (p.Gly1099Arg)
NM_014795.4(ZEB2):c.3311C>T (p.Thr1104Ile)
NM_014795.4(ZEB2):c.3337T>A (p.Leu1113Met) rs730881204
NM_014795.4(ZEB2):c.3444C>T (p.Tyr1148=) rs374141392
NM_014795.4(ZEB2):c.3459A>G (p.Arg1153=) rs1573707737
NM_014795.4(ZEB2):c.3489A>G (p.Glu1163=) rs1573707668
NM_014795.4(ZEB2):c.3495A>G (p.Glu1165=) rs907774736
NM_014795.4(ZEB2):c.403+10G>A rs1573739611
NM_014795.4(ZEB2):c.462G>A (p.Glu154=) rs372940559
NM_014795.4(ZEB2):c.471T>C (p.Asp157=) rs775694100
NM_014795.4(ZEB2):c.593-9C>T rs372216323
NM_014795.4(ZEB2):c.621T>C (p.Phe207=) rs934470843
NM_014795.4(ZEB2):c.696C>T (p.Tyr232=) rs1060503990
NM_014795.4(ZEB2):c.720C>T (p.Asn240=) rs1022840384
NM_014795.4(ZEB2):c.759C>T (p.Arg253=) rs150853991
NM_014795.4(ZEB2):c.798G>A (p.Gly266=) rs34961586
NM_014795.4(ZEB2):c.807+8G>A rs367991951
NM_014795.4(ZEB2):c.82_87del (p.Tyr28_Asp29del) rs730881214

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.