ClinVar Miner

List of variants in gene ZEB2 reported by CeGaT Center for Human Genetics Tuebingen

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Gene type:
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Total variants: 77
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HGVS dbSNP gnomAD frequency
NM_014795.4(ZEB2):c.930C>T (p.Tyr310=) rs6711223 0.01102
NM_014795.4(ZEB2):c.2141C>T (p.Pro714Leu) rs112581563 0.00281
NM_014795.4(ZEB2):c.489C>T (p.Ile163=) rs138859323 0.00277
NM_014795.4(ZEB2):c.-69-729A>C rs538269684 0.00255
NM_014795.4(ZEB2):c.1480C>T (p.Pro494Ser) rs144952836 0.00206
NM_014795.4(ZEB2):c.807+3G>C rs144925893 0.00194
NM_014795.4(ZEB2):c.2230A>G (p.Ile744Val) rs112005830 0.00087
NM_014795.4(ZEB2):c.1161A>G (p.Leu387=) rs146673563 0.00084
NM_014795.4(ZEB2):c.798G>C (p.Gly266=) rs34961586 0.00078
NM_014795.4(ZEB2):c.1306A>G (p.Met436Val) rs145812868 0.00052
NM_014795.4(ZEB2):c.1276T>A (p.Leu426Ile) rs201881288 0.00036
NM_014795.4(ZEB2):c.759C>T (p.Arg253=) rs150853991 0.00033
NM_014795.4(ZEB2):c.304A>T (p.Ile102Phe) rs201109457 0.00022
NM_014795.4(ZEB2):c.1848T>G (p.Pro616=) rs144835963 0.00014
NM_014795.4(ZEB2):c.2457A>G (p.Ser819=) rs144184948 0.00014
NM_014795.4(ZEB2):c.2973C>T (p.Ile991=) rs572507342 0.00014
NM_014795.4(ZEB2):c.3640A>G (p.Met1214Val) rs199951665 0.00014
NM_014795.4(ZEB2):c.2084G>A (p.Arg695Gln) rs147693839 0.00012
NM_014795.4(ZEB2):c.1587G>A (p.Thr529=) rs148709333 0.00010
NM_014795.4(ZEB2):c.1221C>T (p.His407=) rs144613207 0.00006
NM_014795.4(ZEB2):c.3432C>T (p.Gly1144=) rs768007761 0.00004
NM_014795.4(ZEB2):c.374C>T (p.Thr125Met) rs727504227 0.00004
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.1836G>A (p.Ala612=) rs754916469 0.00003
NM_014795.4(ZEB2):c.807+8G>A rs367991951 0.00003
NM_014795.4(ZEB2):c.309A>G (p.Leu103=) rs187331667 0.00002
NM_014795.4(ZEB2):c.2043G>A (p.Val681=) rs769391382 0.00001
NM_014795.4(ZEB2):c.2124G>A (p.Leu708=) rs1289485468 0.00001
NM_014795.4(ZEB2):c.2256G>A (p.Thr752=) rs772121083 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.3204C>G (p.Gly1068=) rs565634569 0.00001
NM_014795.4(ZEB2):c.324T>C (p.Asp108=) rs148117680 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.697C>T (p.Arg233Cys) rs1303138587 0.00001
NM_014795.4(ZEB2):c.726C>T (p.Ser242=) rs929943753 0.00001
NC_000002.12:g.144520475_144520477dup rs1303890891
NM_014795.4(ZEB2):c.*1992T>C rs558354594
NM_014795.4(ZEB2):c.*2377GT[7] rs886054884
NM_014795.4(ZEB2):c.*2387G>A
NM_014795.4(ZEB2):c.*2518G>T rs138683759
NM_014795.4(ZEB2):c.*2525dup rs886054882
NM_014795.4(ZEB2):c.-69-1G>C rs587776612
NM_014795.4(ZEB2):c.1143G>T (p.Met381Ile)
NM_014795.4(ZEB2):c.1183C>G (p.Leu395Val) rs1288005424
NM_014795.4(ZEB2):c.1342C>T (p.Leu448Phe)
NM_014795.4(ZEB2):c.1408dup (p.Thr470fs)
NM_014795.4(ZEB2):c.1542G>T (p.Pro514=) rs141674976
NM_014795.4(ZEB2):c.157_158delinsTT (p.Ala53Phe)
NM_014795.4(ZEB2):c.1630dup (p.Thr544fs) rs1703279692
NM_014795.4(ZEB2):c.1875C>T (p.Ala625=) rs752759296
NM_014795.4(ZEB2):c.1928A>G (p.Lys643Arg)
NM_014795.4(ZEB2):c.2025G>A (p.Leu675=)
NM_014795.4(ZEB2):c.2181A>G (p.Leu727=)
NM_014795.4(ZEB2):c.2417_2432del (p.Phe806fs)
NM_014795.4(ZEB2):c.2752C>T (p.Pro918Ser) rs1560605894
NM_014795.4(ZEB2):c.2761C>T (p.Arg921Ter) rs587784566
NM_014795.4(ZEB2):c.2823T>A (p.Thr941=)
NM_014795.4(ZEB2):c.3046C>T (p.Arg1016Ter) rs886041989
NM_014795.4(ZEB2):c.3150G>A (p.Ser1050=)
NM_014795.4(ZEB2):c.318T>A (p.Ser106=) rs1295409839
NM_014795.4(ZEB2):c.3218A>G (p.His1073Arg) rs1703133873
NM_014795.4(ZEB2):c.3307C>A (p.Pro1103Thr)
NM_014795.4(ZEB2):c.338T>C (p.Met113Thr) rs758065125
NM_014795.4(ZEB2):c.3480C>T (p.Phe1160=) rs1280059432
NM_014795.4(ZEB2):c.3G>A (p.Met1Ile)
NM_014795.4(ZEB2):c.470A>G (p.Asp157Gly) rs761041545
NM_014795.4(ZEB2):c.73+3504C>T
NM_014795.4(ZEB2):c.73+3513A>G
NM_014795.4(ZEB2):c.73+3538G>A
NM_014795.4(ZEB2):c.73+3569T>C
NM_014795.4(ZEB2):c.747G>C (p.Thr249=)
NM_014795.4(ZEB2):c.753C>T (p.Ala251=)
NM_014795.4(ZEB2):c.881A>C (p.Lys294Thr) rs2149877956
NM_014795.4(ZEB2):c.971C>T (p.Ser324Phe)

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