ClinVar Miner

List of variants in gene ZEB2 reported by Genetic Services Laboratory, University of Chicago

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 55
Download table as spreadsheet
HGVS dbSNP
NM_014795.4(ZEB2):c.1027C>T (p.Arg343Ter) rs786204815
NM_014795.4(ZEB2):c.1106T>A (p.Leu369Ter) rs797046117
NM_014795.4(ZEB2):c.1161A>G (p.Leu387=) rs146673563
NM_014795.4(ZEB2):c.1276T>A (p.Leu426Ile) rs201881288
NM_014795.4(ZEB2):c.1410T>A (p.Thr470=) rs34890427
NM_014795.4(ZEB2):c.1426dup (p.Met476fs) rs587776604
NM_014795.4(ZEB2):c.1438G>T (p.Ala480Ser) rs143854197
NM_014795.4(ZEB2):c.1480C>T (p.Pro494Ser) rs144952836
NM_014795.4(ZEB2):c.1489C>T (p.Gln497Ter) rs1553961702
NM_014795.4(ZEB2):c.1542G>A (p.Pro514=) rs141674976
NM_014795.4(ZEB2):c.1638C>T (p.Asp546=) rs149035844
NM_014795.4(ZEB2):c.1916T>C (p.Val639Ala) rs780637261
NM_014795.4(ZEB2):c.1956C>A (p.Tyr652Ter)
NM_014795.4(ZEB2):c.2061del (p.Phe687fs) rs797046118
NM_014795.4(ZEB2):c.2072G>A (p.Trp691Ter) rs1553961610
NM_014795.4(ZEB2):c.2083C>T (p.Arg695Ter) rs137852981
NM_014795.4(ZEB2):c.2141C>T (p.Pro714Leu) rs112581563
NM_014795.4(ZEB2):c.2142G>A (p.Pro714=) rs201180901
NM_014795.4(ZEB2):c.2162C>T (p.Pro721Leu) rs1240429329
NM_014795.4(ZEB2):c.2203C>T (p.Pro735Ser) rs144154908
NM_014795.4(ZEB2):c.220G>A (p.Val74Met) rs767169568
NM_014795.4(ZEB2):c.2230A>G (p.Ile744Val) rs112005830
NM_014795.4(ZEB2):c.2329C>T (p.His777Tyr) rs587784564
NM_014795.4(ZEB2):c.2352T>C (p.Ser784=) rs201990887
NM_014795.4(ZEB2):c.2361T>C (p.Asn787=) rs201567433
NM_014795.4(ZEB2):c.2404_2407del (p.Thr802fs) rs797046119
NM_014795.4(ZEB2):c.2497A>G (p.Thr833Ala) rs1490526407
NM_014795.4(ZEB2):c.2501del (p.Lys834fs) rs587784565
NM_014795.4(ZEB2):c.2691T>A (p.Ala897=) rs1553961508
NM_014795.4(ZEB2):c.2761C>T (p.Arg921Ter) rs587784566
NM_014795.4(ZEB2):c.2894T>A (p.Leu965Ter) rs797046120
NM_014795.4(ZEB2):c.2973C>T (p.Ile991=) rs572507342
NM_014795.4(ZEB2):c.3067+6A>T rs143450927
NM_014795.4(ZEB2):c.309A>G (p.Leu103=) rs187331667
NM_014795.4(ZEB2):c.3109A>T (p.Lys1037Ter) rs1553960793
NM_014795.4(ZEB2):c.3137C>A (p.Ser1046Ter) rs797046121
NM_014795.4(ZEB2):c.3141G>C (p.Arg1047Ser) rs587784567
NM_014795.4(ZEB2):c.3304G>A (p.Glu1102Lys) rs1553960767
NM_014795.4(ZEB2):c.332-6C>T rs730881186
NM_014795.4(ZEB2):c.3444C>T (p.Tyr1148=) rs374141392
NM_014795.4(ZEB2):c.462G>A (p.Glu154=) rs372940559
NM_014795.4(ZEB2):c.466C>T (p.Arg156Cys) rs147021269
NM_014795.4(ZEB2):c.489C>T (p.Ile163=) rs138859323
NM_014795.4(ZEB2):c.674C>A (p.Ser225Ter) rs797046122
NM_014795.4(ZEB2):c.702C>T (p.His234=) rs140169964
NM_014795.4(ZEB2):c.746C>T (p.Thr249Met) rs1248212141
NM_014795.4(ZEB2):c.747G>A (p.Thr249=) rs587784569
NM_014795.4(ZEB2):c.798G>C (p.Gly266=) rs34961586
NM_014795.4(ZEB2):c.808-4A>G rs759097764
NM_014795.4(ZEB2):c.823C>T (p.Gln275Ter) rs587784570
NM_014795.4(ZEB2):c.904C>T (p.Arg302Ter) rs587784571
NM_014795.4(ZEB2):c.917-21T>C rs35213774
NM_014795.4(ZEB2):c.930C>T (p.Tyr310=) rs6711223
NM_014795.4(ZEB2):c.9G>A (p.Gln3=) rs149882004
NM_014795.4(ZEB2):c.9G>C (p.Gln3His) rs149882004

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.