List of variants in gene ZEB2 reported as likely pathogenic for central nervous system disorder

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 37

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_014795.4(ZEB2):c.-69-2A>C
NM_014795.4(ZEB2):c.1168del (p.Ile390fs)	rs1553961747
NM_014795.4(ZEB2):c.1683_1689dup (p.Asp564fs)	rs1703278635
NM_014795.4(ZEB2):c.1884del (p.Phe628fs)	rs786204811
NM_014795.4(ZEB2):c.2180del (p.Leu727fs)	rs786204810
NM_014795.4(ZEB2):c.2273_2274del (p.Leu758fs)
NM_014795.4(ZEB2):c.2384del (p.Asn795fs)	rs2149876640
NM_014795.4(ZEB2):c.247dup (p.Glu83fs)	rs1553964145
NM_014795.4(ZEB2):c.2865C>G (p.Tyr955Ter)	rs2149876315
NM_014795.4(ZEB2):c.2866C>T (p.Gln956Ter)
NM_014795.4(ZEB2):c.2890G>T (p.Glu964Ter)
NM_014795.4(ZEB2):c.2932G>T (p.Asp978Tyr)	rs863224942
NM_014795.4(ZEB2):c.2973del (p.Lys992fs)	rs1703231315
NM_014795.4(ZEB2):c.3023T>G (p.Phe1008Cys)	rs1553961332
NM_014795.4(ZEB2):c.3046C>T (p.Arg1016Ter)	rs886041989
NM_014795.4(ZEB2):c.3067+2T>G
NM_014795.4(ZEB2):c.3095del (p.Cys1032fs)	rs1060500653
NM_014795.4(ZEB2):c.3118C>T (p.His1040Tyr)	rs1553960788
NM_014795.4(ZEB2):c.3122A>G (p.His1041Arg)	rs1573708153
NM_014795.4(ZEB2):c.3133C>T (p.His1045Tyr)	rs1703135134
NM_014795.4(ZEB2):c.3146A>G (p.His1049Arg)	rs1114167349
NM_014795.4(ZEB2):c.3160C>G (p.Pro1054Ala)
NM_014795.4(ZEB2):c.3164A>G (p.Tyr1055Cys)	rs1135402759
NM_014795.4(ZEB2):c.3200C>A (p.Ser1067Ter)	rs1423851170
NM_014795.4(ZEB2):c.3214C>T (p.Gln1072Ter)	rs1703133912
NM_014795.4(ZEB2):c.3227dup (p.His1076fs)
NM_014795.4(ZEB2):c.329del (p.Pro110fs)
NM_014795.4(ZEB2):c.332-3C>G
NM_014795.4(ZEB2):c.441C>G (p.Tyr147Ter)
NM_014795.4(ZEB2):c.639C>A (p.Cys213Ter)	rs1451961075
NM_014795.4(ZEB2):c.66del (p.Asn24fs)	rs2149935119
NM_014795.4(ZEB2):c.73+2T>C	rs398124282
NM_014795.4(ZEB2):c.851G>A (p.Cys284Tyr)	rs1703306516
NM_014795.4(ZEB2):c.876dup (p.Tyr293fs)	rs2149877962
NM_014795.4(ZEB2):c.899A>G (p.His300Arg)	rs1573718595
NM_014795.4(ZEB2):c.916+1G>T	rs2149877941
NM_014795.4(ZEB2):c.917G>A (p.Gly306Asp)	rs1703292916

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.