ClinVar Miner

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

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Gene type:
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Total variants: 106
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HGVS dbSNP gnomAD frequency
NM_014795.4(ZEB2):c.2084G>A (p.Arg695Gln) rs147693839 0.00012
NM_014795.4(ZEB2):c.3219C>T (p.His1073=) rs139944383 0.00009
NM_014795.4(ZEB2):c.2855G>C (p.Arg952Thr) rs151256895 0.00006
NM_014795.4(ZEB2):c.219C>T (p.His73=) rs778851716 0.00005
NM_014795.4(ZEB2):c.374C>T (p.Thr125Met) rs727504227 0.00004
NM_014795.4(ZEB2):c.-9C>T rs730881183 0.00003
NM_014795.4(ZEB2):c.1655G>A (p.Ser552Asn) rs1441120961 0.00003
NM_014795.4(ZEB2):c.167T>C (p.Leu56Pro) rs61750440 0.00003
NM_014795.4(ZEB2):c.2886+4A>C rs754532627 0.00003
NM_014795.4(ZEB2):c.403+9T>C rs886042422 0.00003
NM_014795.4(ZEB2):c.2766A>T (p.Pro922=) rs185223937 0.00002
NM_014795.4(ZEB2):c.1877G>A (p.Gly626Glu) rs794727923 0.00001
NM_014795.4(ZEB2):c.1880T>A (p.Val627Asp) rs730881176 0.00001
NM_014795.4(ZEB2):c.2004G>T (p.Glu668Asp) rs767506087 0.00001
NM_014795.4(ZEB2):c.2365T>C (p.Ser789Pro) rs730881197 0.00001
NM_014795.4(ZEB2):c.2390A>G (p.His797Arg) rs201227541 0.00001
NM_014795.4(ZEB2):c.2497A>G (p.Thr833Ala) rs1490526407 0.00001
NM_014795.4(ZEB2):c.2602G>A (p.Glu868Lys) rs921397888 0.00001
NM_014795.4(ZEB2):c.26G>A (p.Gly9Asp) rs1242134764 0.00001
NM_014795.4(ZEB2):c.3329G>A (p.Arg1110Gln) rs1346483037 0.00001
NM_014795.4(ZEB2):c.3353C>A (p.Pro1118His) rs780004720 0.00001
NM_014795.4(ZEB2):c.388A>G (p.Ile130Val) rs1057520175 0.00001
NM_014795.4(ZEB2):c.467G>A (p.Arg156His) rs1250217464 0.00001
NM_014795.4(ZEB2):c.773G>A (p.Arg258Gln) rs730881173 0.00001
GRCh37/hg19 2q22.3(chr2:145235108-145292497)x1
NM_014795.4(ZEB2):c.-69-9G>C rs2149935270
NM_014795.4(ZEB2):c.113C>T (p.Thr38Ile) rs2149891283
NM_014795.4(ZEB2):c.1183C>G (p.Leu395Val) rs1288005424
NM_014795.4(ZEB2):c.1199A>G (p.Tyr400Cys)
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.1317A>C (p.Leu439Phe) rs2149877328
NM_014795.4(ZEB2):c.1342C>T (p.Leu448Phe)
NM_014795.4(ZEB2):c.1446A>C (p.Glu482Asp) rs886043609
NM_014795.4(ZEB2):c.1534G>T (p.Gly512Cys) rs141781307
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.1592A>T (p.Glu531Val)
NM_014795.4(ZEB2):c.1681A>G (p.Thr561Ala) rs730881195
NM_014795.4(ZEB2):c.1687A>G (p.Ile563Val)
NM_014795.4(ZEB2):c.1835C>A (p.Ala612Glu)
NM_014795.4(ZEB2):c.1862T>C (p.Val621Ala) rs2149877024
NM_014795.4(ZEB2):c.18G>A (p.Met6Ile)
NM_014795.4(ZEB2):c.1927_1934delinsGG (p.Lys643_Met645delinsGly) rs796065335
NM_014795.4(ZEB2):c.1994T>C (p.Met665Thr) rs1703272747
NM_014795.4(ZEB2):c.2281A>T (p.Thr761Ser) rs867243713
NM_014795.4(ZEB2):c.246GGAAGA[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.2624T>G (p.Leu875Arg) rs730881199
NM_014795.4(ZEB2):c.2641A>C (p.Asn881His) rs794727922
NM_014795.4(ZEB2):c.2677C>A (p.Pro893Thr)
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.2740C>A (p.Gln914Lys)
NM_014795.4(ZEB2):c.2792T>G (p.Phe931Cys) rs2149876375
NM_014795.4(ZEB2):c.2808C>T (p.Ala936=) rs749708858
NM_014795.4(ZEB2):c.2847G>A (p.Met949Ile) rs1703257497
NM_014795.4(ZEB2):c.2899G>A (p.Asp967Asn) rs1703232514
NM_014795.4(ZEB2):c.2950T>C (p.Ser984Pro) rs2149875549
NM_014795.4(ZEB2):c.298A>C (p.Asn100His)
NM_014795.4(ZEB2):c.3036T>G (p.Ser1012Arg) rs2149875491
NM_014795.4(ZEB2):c.3047G>A (p.Arg1016Gln) rs2149875484
NM_014795.4(ZEB2):c.3068-3C>G rs1703135967
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.3149C>T (p.Ser1050Leu) rs1226638635
NM_014795.4(ZEB2):c.314C>G (p.Ala105Gly)
NM_014795.4(ZEB2):c.3188G>A (p.Arg1063His)
NM_014795.4(ZEB2):c.3206C>G (p.Ser1069Trp) rs1553960778
NM_014795.4(ZEB2):c.3206C>T (p.Ser1069Leu)
NM_014795.4(ZEB2):c.323_324delinsGA (p.Asp108Gly) rs2149891130
NM_014795.4(ZEB2):c.3277C>G (p.Arg1093Gly) rs730881203
NM_014795.4(ZEB2):c.3307C>A (p.Pro1103Thr)
NM_014795.4(ZEB2):c.3341A>G (p.Gln1114Arg)
NM_014795.4(ZEB2):c.3352C>T (p.Pro1118Ser) rs2149872541
NM_014795.4(ZEB2):c.3353C>T (p.Pro1118Leu) rs780004720
NM_014795.4(ZEB2):c.3365C>G (p.Ser1122Cys)
NM_014795.4(ZEB2):c.338T>C (p.Met113Thr) rs758065125
NM_014795.4(ZEB2):c.3409G>A (p.Glu1137Lys) rs730881205
NM_014795.4(ZEB2):c.3454G>C (p.Gly1152Arg) rs1480636573
NM_014795.4(ZEB2):c.3469G>A (p.Asp1157Asn) rs1573707719
NM_014795.4(ZEB2):c.422C>T (p.Thr141Ile) rs1703366182
NM_014795.4(ZEB2):c.437A>G (p.Glu146Gly)
NM_014795.4(ZEB2):c.470A>G (p.Asp157Gly) rs761041545
NM_014795.4(ZEB2):c.476A>G (p.His159Arg) rs2149879723
NM_014795.4(ZEB2):c.477T>G (p.His159Gln) rs730881188
NM_014795.4(ZEB2):c.479C>G (p.Ala160Gly) rs2149879719
NM_014795.4(ZEB2):c.652C>T (p.Arg218Trp)
NM_014795.4(ZEB2):c.664C>T (p.Arg222Cys) rs730881189
NM_014795.4(ZEB2):c.753C>T (p.Ala251=)
NM_014795.4(ZEB2):c.757C>A (p.Arg253Ser) rs760301787
NM_014795.4(ZEB2):c.769G>A (p.Glu257Lys)
NM_014795.4(ZEB2):c.807+3G>T rs144925893
NM_014795.4(ZEB2):c.839G>A (p.Arg280His) rs2149877979
NM_014795.4(ZEB2):c.850T>C (p.Cys284Arg)
NM_014795.4(ZEB2):c.860G>A (p.Cys287Tyr) rs2149877974
NM_014795.4(ZEB2):c.865A>G (p.Lys289Glu) rs1064793305
NM_014795.4(ZEB2):c.881A>C (p.Lys294Thr) rs2149877956
NM_014795.4(ZEB2):c.905G>A (p.Arg302Gln) rs730881174
NM_014795.4(ZEB2):c.916+4A>T
NM_014795.4(ZEB2):c.925C>T (p.Pro309Ser) rs1085307638
NM_014795.4(ZEB2):c.953G>A (p.Arg318His) rs2149877534
NM_014795.4(ZEB2):c.962A>C (p.His321Pro) rs730881191
NM_014795.4(ZEB2):c.962A>G (p.His321Arg)
NM_014795.4(ZEB2):c.9G>A (p.Gln3=) rs149882004

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