ClinVar Miner

List of variants in gene ZEB2 reported as benign by Invitae

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Gene type:
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Total variants: 43
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HGVS dbSNP
NM_014795.4(ZEB2):c.10C>G (p.Pro4Ala) rs146394306
NM_014795.4(ZEB2):c.1161A>G (p.Leu387=) rs146673563
NM_014795.4(ZEB2):c.1336C>T (p.Pro446Ser) rs1435380197
NM_014795.4(ZEB2):c.139G>T (p.Ala47Ser) rs730881184
NM_014795.4(ZEB2):c.1410T>A (p.Thr470=) rs34890427
NM_014795.4(ZEB2):c.1587G>A (p.Thr529=) rs148709333
NM_014795.4(ZEB2):c.1840C>T (p.Leu614=) rs145201706
NM_014795.4(ZEB2):c.1993A>G (p.Met665Val) rs1388932284
NM_014795.4(ZEB2):c.2084G>A (p.Arg695Gln) rs147693839
NM_014795.4(ZEB2):c.2119T>A (p.Ser707Thr)
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.2203C>T (p.Pro735Ser) rs144154908
NM_014795.4(ZEB2):c.2205T>C (p.Pro735=) rs149964599
NM_014795.4(ZEB2):c.2230A>G (p.Ile744Val) rs112005830
NM_014795.4(ZEB2):c.2248A>G (p.Ser750Gly) rs730881196
NM_014795.4(ZEB2):c.224G>A (p.Ser75Asn)
NM_014795.4(ZEB2):c.2361T>C (p.Asn787=) rs201567433
NM_014795.4(ZEB2):c.242G>C (p.Arg81Thr)
NM_014795.4(ZEB2):c.2538T>A (p.His846Gln) rs557767273
NM_014795.4(ZEB2):c.2565C>G (p.Asn855Lys) rs904620951
NM_014795.4(ZEB2):c.2804T>C (p.Met935Thr) rs201902790
NM_014795.4(ZEB2):c.2887-4G>A rs147972125
NM_014795.4(ZEB2):c.2973C>T (p.Ile991=) rs572507342
NM_014795.4(ZEB2):c.297C>T (p.Asn99=) rs147603619
NM_014795.4(ZEB2):c.304A>T (p.Ile102Phe) rs201109457
NM_014795.4(ZEB2):c.3067+6A>T rs143450927
NM_014795.4(ZEB2):c.3285G>A (p.Ala1095=) rs201630448
NM_014795.4(ZEB2):c.3327C>A (p.Asn1109Lys) rs1288140327
NM_014795.4(ZEB2):c.3471C>T (p.Asp1157=) rs149526010
NM_014795.4(ZEB2):c.3536T>C (p.Ile1179Thr) rs1238900874
NM_014795.4(ZEB2):c.374C>T (p.Thr125Met) rs727504227
NM_014795.4(ZEB2):c.375G>A (p.Thr125=) rs138389836
NM_014795.4(ZEB2):c.395A>G (p.Asn132Ser) rs369622877
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.798G>C (p.Gly266=) rs34961586
NM_014795.4(ZEB2):c.807+3G>A rs144925893
NM_014795.4(ZEB2):c.807+3G>C rs144925893
NM_014795.4(ZEB2):c.930C>T (p.Tyr310=) rs6711223
NM_014795.4(ZEB2):c.981G>A (p.Ser327=) rs201579452
NM_014795.4(ZEB2):c.9G>A (p.Gln3=) rs149882004
NM_014795.4(ZEB2):c.9G>C (p.Gln3His) rs149882004

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