ClinVar Miner

List of variants in gene ZEB2 reported as likely benign by Ambry Genetics

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Gene type:
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Total variants: 59
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HGVS dbSNP gnomAD frequency
NM_014795.4(ZEB2):c.489C>T (p.Ile163=) rs138859323 0.00277
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.2205T>C (p.Pro735=) rs149964599 0.00062
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.2601G>A (p.Lys867=) rs139369265 0.00029
NM_014795.4(ZEB2):c.462G>A (p.Glu154=) rs372940559 0.00023
NM_014795.4(ZEB2):c.304A>T (p.Ile102Phe) rs201109457 0.00022
NM_014795.4(ZEB2):c.10C>G (p.Pro4Ala) rs146394306 0.00015
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.1840C>T (p.Leu614=) rs145201706 0.00011
NM_014795.4(ZEB2):c.3219C>T (p.His1073=) rs139944383 0.00009
NM_014795.4(ZEB2):c.297C>T (p.Asn99=) rs147603619 0.00007
NM_014795.4(ZEB2):c.1221C>T (p.His407=) rs144613207 0.00006
NM_014795.4(ZEB2):c.2275A>G (p.Arg759Gly) rs748354087 0.00006
NM_014795.4(ZEB2):c.2361T>C (p.Asn787=) rs201567433 0.00006
NM_014795.4(ZEB2):c.219C>T (p.His73=) rs778851716 0.00005
NM_014795.4(ZEB2):c.1482A>G (p.Pro494=) rs375275148 0.00004
NM_014795.4(ZEB2):c.1527G>A (p.Pro509=) rs759999662 0.00004
NM_014795.4(ZEB2):c.3432C>T (p.Gly1144=) rs768007761 0.00004
NM_014795.4(ZEB2):c.3451C>A (p.Leu1151Met) rs772764893 0.00004
NM_014795.4(ZEB2):c.768C>T (p.Leu256=) rs370751674 0.00004
NM_014795.4(ZEB2):c.180G>A (p.Thr60=) rs372888487 0.00003
NM_014795.4(ZEB2):c.1836G>A (p.Ala612=) rs754916469 0.00003
NM_014795.4(ZEB2):c.2255C>T (p.Thr752Met) rs143438888 0.00003
NM_014795.4(ZEB2):c.225C>T (p.Ser75=) rs754754722 0.00003
NM_014795.4(ZEB2):c.2215A>G (p.Ile739Val) rs730881178 0.00002
NM_014795.4(ZEB2):c.2766A>T (p.Pro922=) rs185223937 0.00002
NM_014795.4(ZEB2):c.3466G>T (p.Gly1156Cys) rs776351453 0.00002
NM_014795.4(ZEB2):c.981G>A (p.Ser327=) rs201579452 0.00002
NM_014795.4(ZEB2):c.150C>T (p.Asp50=) rs587780996 0.00001
NM_014795.4(ZEB2):c.1554T>C (p.His518=) rs1431508601 0.00001
NM_014795.4(ZEB2):c.2256G>A (p.Thr752=) rs772121083 0.00001
NM_014795.4(ZEB2):c.2742G>A (p.Gln914=) rs780189288 0.00001
NM_014795.4(ZEB2):c.2935A>G (p.Met979Val) rs777220598 0.00001
NM_014795.4(ZEB2):c.3264G>A (p.Arg1088=) rs774763773 0.00001
NM_014795.4(ZEB2):c.385G>A (p.Ala129Thr) rs730881187 0.00001
NM_014795.4(ZEB2):c.1092A>C (p.Ser364=) rs1560607402
NM_014795.4(ZEB2):c.1410T>A (p.Thr470=) rs34890427
NM_014795.4(ZEB2):c.1534G>A (p.Gly512Ser) rs141781307
NM_014795.4(ZEB2):c.166C>T (p.Leu56=)
NM_014795.4(ZEB2):c.1908G>T (p.Leu636Phe)
NM_014795.4(ZEB2):c.2205_2206delinsCG (p.Met736Val) rs1060500654
NM_014795.4(ZEB2):c.2255C>G (p.Thr752Arg) rs143438888
NM_014795.4(ZEB2):c.2313A>G (p.Pro771=) rs1560606324
NM_014795.4(ZEB2):c.2517T>C (p.Ala839=)
NM_014795.4(ZEB2):c.2589T>C (p.Thr863=) rs985918539
NM_014795.4(ZEB2):c.3308C>G (p.Pro1103Arg)
NM_014795.4(ZEB2):c.3312C>T (p.Thr1104=) rs1403782189
NM_014795.4(ZEB2):c.624C>T (p.Ala208=) rs1451197588
NM_014795.4(ZEB2):c.660C>T (p.Tyr220=)
NM_014795.4(ZEB2):c.702C>T (p.His234=) rs140169964
NM_014795.4(ZEB2):c.762C>T (p.Thr254=) rs771709950
NM_014795.4(ZEB2):c.807+3G>A rs144925893
NM_014795.4(ZEB2):c.915T>C (p.Ser305=)

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