ClinVar Miner

List of variants in gene ZEB2 reported as likely benign by Invitae

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Gene type:
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Total variants: 29
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HGVS dbSNP
NM_014795.3(ZEB2):c.1053T>C (p.Gly351=) rs1553961766
NM_014795.3(ZEB2):c.1071T>G (p.Val357=) rs200510665
NM_014795.3(ZEB2):c.1221C>T (p.His407=) rs144613207
NM_014795.3(ZEB2):c.1276T>A (p.Leu426Ile) rs201881288
NM_014795.3(ZEB2):c.1315T>C (p.Leu439=) rs1060503991
NM_014795.3(ZEB2):c.1386G>C (p.Lys462Asn) rs780523431
NM_014795.3(ZEB2):c.1438G>T (p.Ala480Ser) rs143854197
NM_014795.3(ZEB2):c.1480C>T (p.Pro494Ser) rs144952836
NM_014795.3(ZEB2):c.1503A>G (p.Gln501=) rs1269576350
NM_014795.3(ZEB2):c.1542G>T (p.Pro514=) rs141674976
NM_014795.3(ZEB2):c.1638C>T (p.Asp546=) rs149035844
NM_014795.3(ZEB2):c.168G>C (p.Leu56=) rs1553964156
NM_014795.3(ZEB2):c.1836G>A (p.Ala612=) rs754916469
NM_014795.3(ZEB2):c.2016T>C (p.Asp672=) rs1057522531
NM_014795.3(ZEB2):c.2120C>T (p.Ser707Phe) rs1174325176
NM_014795.3(ZEB2):c.216A>C (p.Pro72=) rs764560219
NM_014795.3(ZEB2):c.2205_2206delTAinsCG (p.Met736Val) rs1060500654
NM_014795.3(ZEB2):c.2215A>G (p.Ile739Val) rs730881178
NM_014795.3(ZEB2):c.2325G>A (p.Leu775=) rs1553961560
NM_014795.3(ZEB2):c.2457A>G (p.Ser819=) rs144184948
NM_014795.3(ZEB2):c.2646A>G (p.Pro882=) rs372224804
NM_014795.3(ZEB2):c.2766A>T (p.Pro922=) rs185223937
NM_014795.3(ZEB2):c.30C>T (p.Pro10=) rs747483109
NM_014795.3(ZEB2):c.324T>C (p.Asp108=) rs148117680
NM_014795.3(ZEB2):c.462G>A (p.Glu154=) rs372940559
NM_014795.3(ZEB2):c.593-9C>T rs372216323
NM_014795.3(ZEB2):c.696C>T (p.Tyr232=) rs1060503990
NM_014795.3(ZEB2):c.759C>T (p.Arg253=) rs150853991
NM_014795.3(ZEB2):c.807+8G>A rs367991951

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