ClinVar Miner

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

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Gene type:
ClinVar version:
Total variants: 34
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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.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.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.3640A>G (p.Met1214Val) rs199951665 0.00014
NM_014795.4(ZEB2):c.2084G>A (p.Arg695Gln) rs147693839 0.00012
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.309A>G (p.Leu103=) rs187331667 0.00002
NM_014795.4(ZEB2):c.2043G>A (p.Val681=) rs769391382 0.00001
NM_014795.4(ZEB2):c.324T>C (p.Asp108=) rs148117680 0.00001
NM_014795.4(ZEB2):c.726C>T (p.Ser242=) rs929943753 0.00001
NM_014795.4(ZEB2):c.*1992T>C rs558354594
NM_014795.4(ZEB2):c.*2387G>A
NM_014795.4(ZEB2):c.*2525dup rs886054882
NM_014795.4(ZEB2):c.1875C>T (p.Ala625=) rs752759296
NM_014795.4(ZEB2):c.2025G>A (p.Leu675=)
NM_014795.4(ZEB2):c.2181A>G (p.Leu727=)
NM_014795.4(ZEB2):c.2752C>T (p.Pro918Ser) rs1560605894
NM_014795.4(ZEB2):c.2823T>A (p.Thr941=)
NM_014795.4(ZEB2):c.318T>A (p.Ser106=) rs1295409839
NM_014795.4(ZEB2):c.3480C>T (p.Phe1160=) rs1280059432
NM_014795.4(ZEB2):c.73+3504C>T
NM_014795.4(ZEB2):c.73+3538G>A
NM_014795.4(ZEB2):c.73+3569T>C

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