ClinVar Miner

List of variants in gene ZEB2 reported as uncertain significance by Invitae

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 50
Download table as spreadsheet
HGVS dbSNP
NM_014795.3(ZEB2):c.10C>G (p.Pro4Ala) rs146394306
NM_014795.3(ZEB2):c.1222G>A (p.Gly408Arg)
NM_014795.3(ZEB2):c.1309C>A (p.Gln437Lys) rs760437173
NM_014795.3(ZEB2):c.139G>T (p.Ala47Ser) rs730881184
NM_014795.3(ZEB2):c.1426A>C (p.Met476Leu) rs778246270
NM_014795.3(ZEB2):c.1491A>C (p.Gln497His) rs200378546
NM_014795.3(ZEB2):c.1571G>A (p.Ser524Asn)
NM_014795.3(ZEB2):c.1735A>G (p.Thr579Ala) rs140593583
NM_014795.3(ZEB2):c.179C>T (p.Thr60Met) rs780890592
NM_014795.3(ZEB2):c.1845G>T (p.Gln615His)
NM_014795.3(ZEB2):c.1877G>A (p.Gly626Glu) rs794727923
NM_014795.3(ZEB2):c.1880T>A (p.Val627Asp) rs730881176
NM_014795.3(ZEB2):c.1975C>T (p.Leu659Phe)
NM_014795.3(ZEB2):c.1993A>G (p.Met665Val) rs1388932284
NM_014795.3(ZEB2):c.2248A>G (p.Ser750Gly) rs730881196
NM_014795.3(ZEB2):c.2255C>T (p.Thr752Met) rs143438888
NM_014795.3(ZEB2):c.2327A>G (p.Asp776Gly) rs1553961558
NM_014795.3(ZEB2):c.2354C>G (p.Pro785Arg)
NM_014795.3(ZEB2):c.2390A>G (p.His797Arg)
NM_014795.3(ZEB2):c.2418C>A (p.Phe806Leu)
NM_014795.3(ZEB2):c.2471T>C (p.Met824Thr) rs1553961536
NM_014795.3(ZEB2):c.2497A>G (p.Thr833Ala) rs1490526407
NM_014795.3(ZEB2):c.2541C>A (p.Asn847Lys)
NM_014795.3(ZEB2):c.2545G>A (p.Val849Ile)
NM_014795.3(ZEB2):c.2621A>C (p.Asn874Thr) rs1477010525
NM_014795.3(ZEB2):c.2622T>A (p.Asn874Lys) rs745927130
NM_014795.3(ZEB2):c.2641A>C (p.Asn881His) rs794727922
NM_014795.3(ZEB2):c.2762G>A (p.Arg921Gln) rs147716561
NM_014795.3(ZEB2):c.2774G>A (p.Gly925Glu)
NM_014795.3(ZEB2):c.2855G>C (p.Arg952Thr) rs151256895
NM_014795.3(ZEB2):c.2869C>T (p.Arg957Trp) rs1354236085
NM_014795.3(ZEB2):c.2870G>A (p.Arg957Gln) rs371509136
NM_014795.3(ZEB2):c.2886+4_2886+5delAA
NM_014795.3(ZEB2):c.2951C>T (p.Ser984Phe) rs143474223
NM_014795.3(ZEB2):c.3202_3207delGGCTCG (p.Gly1068_Ser1069del) rs1553960777
NM_014795.3(ZEB2):c.3267A>C (p.Glu1089Asp) rs1553960775
NM_014795.3(ZEB2):c.3327C>A (p.Asn1109Lys) rs1288140327
NM_014795.3(ZEB2):c.3357G>C (p.Gln1119His) rs1332911302
NM_014795.3(ZEB2):c.3408C>G (p.Ser1136Arg) rs1060500655
NM_014795.3(ZEB2):c.3451C>A (p.Leu1151Met) rs772764893
NM_014795.3(ZEB2):c.3536T>C (p.Ile1179Thr)
NM_014795.3(ZEB2):c.3538C>G (p.Arg1180Gly)
NM_014795.3(ZEB2):c.3575A>C (p.Asp1192Ala) rs752093966
NM_014795.3(ZEB2):c.3599A>G (p.Glu1200Gly)
NM_014795.3(ZEB2):c.3640A>G (p.Met1214Val) rs199951665
NM_014795.3(ZEB2):c.385G>A (p.Ala129Thr) rs730881187
NM_014795.3(ZEB2):c.395A>G (p.Asn132Ser) rs369622877
NM_014795.3(ZEB2):c.467G>A (p.Arg156His) rs1250217464
NM_014795.3(ZEB2):c.703G>A (p.Glu235Lys) rs1553962069
NM_014795.3(ZEB2):c.797G>A (p.Gly266Glu) rs1057522361

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.