List of variants in gene ZEB2 reported as benign by Eurofins NTD LLC (GA)

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: 18

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_014795.4(ZEB2):c.930C>T (p.Tyr310=)	rs6711223	0.01102
NM_014795.4(ZEB2):c.2141C>T (p.Pro714Leu)	rs112581563	0.00281
NM_014795.4(ZEB2):c.489C>T (p.Ile163=)	rs138859323	0.00277
NM_014795.4(ZEB2):c.2887-4G>A	rs147972125	0.00222
NM_014795.4(ZEB2):c.1480C>T (p.Pro494Ser)	rs144952836	0.00206
NM_014795.4(ZEB2):c.807+3G>C	rs144925893	0.00194
NM_014795.4(ZEB2):c.3471C>T (p.Asp1157=)	rs149526010	0.00186
NM_014795.4(ZEB2):c.2230A>G (p.Ile744Val)	rs112005830	0.00087
NM_014795.4(ZEB2):c.1161A>G (p.Leu387=)	rs146673563	0.00084
NM_014795.4(ZEB2):c.798G>C (p.Gly266=)	rs34961586	0.00078
NM_014795.4(ZEB2):c.2206A>G (p.Met736Val)	rs139191491	0.00067
NM_014795.4(ZEB2):c.2205T>C (p.Pro735=)	rs149964599	0.00062
NM_014795.4(ZEB2):c.759C>T (p.Arg253=)	rs150853991	0.00033
NM_014795.4(ZEB2):c.1438G>T (p.Ala480Ser)	rs143854197	0.00026
NM_014795.4(ZEB2):c.2255C>T (p.Thr752Met)	rs143438888	0.00003
NM_014795.4(ZEB2):c.2203C>T (p.Pro735Ser)	rs144154908	0.00001
NM_014795.4(ZEB2):c.1410T>A (p.Thr470=)	rs34890427
NM_014795.4(ZEB2):c.3067+6A>T	rs143450927

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.