ClinVar Miner

List of variants in gene ZEB2 reported as likely benign by Ambry Genetics

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Gene type:
ClinVar version:
Total variants: 28
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HGVS dbSNP
NM_014795.4(ZEB2):c.1092A>C (p.Ser364=) rs1560607402
NM_014795.4(ZEB2):c.1161A>G (p.Leu387=) rs146673563
NM_014795.4(ZEB2):c.1221C>T (p.His407=) rs144613207
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.1410T>A (p.Thr470=) rs34890427
NM_014795.4(ZEB2):c.1438G>T (p.Ala480Ser) rs143854197
NM_014795.4(ZEB2):c.1554T>C (p.His518=) rs1431508601
NM_014795.4(ZEB2):c.1836G>A (p.Ala612=) rs754916469
NM_014795.4(ZEB2):c.1840C>T (p.Leu614=) rs145201706
NM_014795.4(ZEB2):c.2141C>T (p.Pro714Leu) rs112581563
NM_014795.4(ZEB2):c.2205_2206delinsCG (p.Met736Val) rs1060500654
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.2313A>G (p.Pro771=) rs1560606324
NM_014795.4(ZEB2):c.2361T>C (p.Asn787=) rs201567433
NM_014795.4(ZEB2):c.2589T>C (p.Thr863=)
NM_014795.4(ZEB2):c.2766A>T (p.Pro922=) rs185223937
NM_014795.4(ZEB2):c.304A>T (p.Ile102Phe) rs201109457
NM_014795.4(ZEB2):c.3264G>A (p.Arg1088=)
NM_014795.4(ZEB2):c.3312C>T (p.Thr1104=) rs1403782189
NM_014795.4(ZEB2):c.3432C>T (p.Gly1144=) rs768007761
NM_014795.4(ZEB2):c.3640A>G (p.Met1214Val) rs199951665
NM_014795.4(ZEB2):c.489C>T (p.Ile163=) rs138859323
NM_014795.4(ZEB2):c.702C>T (p.His234=) rs140169964
NM_014795.4(ZEB2):c.759C>T (p.Arg253=) rs150853991
NM_014795.4(ZEB2):c.762C>T (p.Thr254=)
NM_014795.4(ZEB2):c.798G>C (p.Gly266=) rs34961586

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