ClinVar Miner

List of variants in gene ZEB2 reported as uncertain significance for not provided

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Total variants: 45
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HGVS dbSNP
GRCh37/hg19 2q22.3(chr2:145235108-145292497)x1
NM_014795.4(ZEB2):c.-9C>T rs730881183
NM_014795.4(ZEB2):c.1280G>T (p.Gly427Val) rs1553961730
NM_014795.4(ZEB2):c.1283T>C (p.Val428Ala) rs730881192
NM_014795.4(ZEB2):c.1446A>C (p.Glu482Asp) rs886043609
NM_014795.4(ZEB2):c.1542G>A (p.Pro514=) rs141674976
NM_014795.4(ZEB2):c.1542G>T (p.Pro514=) rs141674976
NM_014795.4(ZEB2):c.1681A>G (p.Thr561Ala) rs730881195
NM_014795.4(ZEB2):c.1877G>A (p.Gly626Glu) rs794727923
NM_014795.4(ZEB2):c.1927_1934delinsGG (p.Lys643_Met645delinsGly) rs796065335
NM_014795.4(ZEB2):c.2004G>T (p.Glu668Asp) rs767506087
NM_014795.4(ZEB2):c.2084G>A (p.Arg695Gln) rs147693839
NM_014795.4(ZEB2):c.219C>T (p.His73=) rs778851716
NM_014795.4(ZEB2):c.2281A>T (p.Thr761Ser) rs867243713
NM_014795.4(ZEB2):c.2365T>C (p.Ser789Pro) rs730881197
NM_014795.4(ZEB2):c.2390A>G (p.His797Arg)
NM_014795.4(ZEB2):c.246_251GGAAGA[3] (p.Glu84_Glu85dup) rs781664431
NM_014795.4(ZEB2):c.2471T>C (p.Met824Thr) rs1553961536
NM_014795.4(ZEB2):c.2486G>A (p.Ser829Asn) rs730881198
NM_014795.4(ZEB2):c.2602G>A (p.Glu868Lys) rs921397888
NM_014795.4(ZEB2):c.2624T>G (p.Leu875Arg) rs730881199
NM_014795.4(ZEB2):c.2641A>C (p.Asn881His) rs794727922
NM_014795.4(ZEB2):c.2707G>T (p.Ala903Ser) rs730881200
NM_014795.4(ZEB2):c.2729T>C (p.Met910Thr) rs730881201
NM_014795.4(ZEB2):c.2766A>T (p.Pro922=) rs185223937
NM_014795.4(ZEB2):c.2855G>C (p.Arg952Thr) rs151256895
NM_014795.4(ZEB2):c.2886+4A>C rs754532627
NM_014795.4(ZEB2):c.3077_3079del (p.Pro1026del) rs398124279
NM_014795.4(ZEB2):c.3130G>A (p.Glu1044Lys) rs730881202
NM_014795.4(ZEB2):c.3219C>T (p.His1073=) rs139944383
NM_014795.4(ZEB2):c.3277C>G (p.Arg1093Gly) rs730881203
NM_014795.4(ZEB2):c.3329G>A (p.Arg1110Gln) rs1346483037
NM_014795.4(ZEB2):c.3409G>A (p.Glu1137Lys) rs730881205
NM_014795.4(ZEB2):c.3640A>G (p.Met1214Val) rs199951665
NM_014795.4(ZEB2):c.374C>T (p.Thr125Met) rs727504227
NM_014795.4(ZEB2):c.403+9T>C rs886042422
NM_014795.4(ZEB2):c.477T>G (p.His159Gln) rs730881188
NM_014795.4(ZEB2):c.664C>T (p.Arg222Cys) rs730881189
NM_014795.4(ZEB2):c.773G>A (p.Arg258Gln) rs730881173
NM_014795.4(ZEB2):c.807+3G>T rs144925893
NM_014795.4(ZEB2):c.865A>G (p.Lys289Glu) rs1064793305
NM_014795.4(ZEB2):c.905G>A (p.Arg302Gln) rs730881174
NM_014795.4(ZEB2):c.925C>T (p.Pro309Ser) rs1085307638
NM_014795.4(ZEB2):c.962A>C (p.His321Pro) rs730881191
NM_014795.4(ZEB2):c.9G>A (p.Gln3=) rs149882004

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