ClinVar Miner

List of variants in gene ZEB2 reported as uncertain significance by Invitae

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Gene type:
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Total variants: 106
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HGVS dbSNP
NM_014795.4(ZEB2):c.1028G>A (p.Arg343Gln)
NM_014795.4(ZEB2):c.1049C>T (p.Thr350Met) rs975397942
NM_014795.4(ZEB2):c.1091C>T (p.Ser364Leu)
NM_014795.4(ZEB2):c.1130A>C (p.Lys377Thr)
NM_014795.4(ZEB2):c.11C>T (p.Pro4Leu)
NM_014795.4(ZEB2):c.1211T>C (p.Met404Thr)
NM_014795.4(ZEB2):c.1222G>A (p.Gly408Arg) rs770190727
NM_014795.4(ZEB2):c.1288C>T (p.Pro430Ser) rs753804606
NM_014795.4(ZEB2):c.128A>G (p.Lys43Arg)
NM_014795.4(ZEB2):c.1309C>A (p.Gln437Lys) rs760437173
NM_014795.4(ZEB2):c.1354A>G (p.Thr452Ala)
NM_014795.4(ZEB2):c.1426A>C (p.Met476Leu) rs778246270
NM_014795.4(ZEB2):c.1446A>C (p.Glu482Asp) rs886043609
NM_014795.4(ZEB2):c.1471A>T (p.Met491Leu)
NM_014795.4(ZEB2):c.1491A>C (p.Gln497His) rs200378546
NM_014795.4(ZEB2):c.1526C>T (p.Pro509Leu) rs1051563603
NM_014795.4(ZEB2):c.1534G>A (p.Gly512Ser) rs141781307
NM_014795.4(ZEB2):c.1571G>A (p.Ser524Asn) rs1560606972
NM_014795.4(ZEB2):c.1601A>G (p.Asn534Ser)
NM_014795.4(ZEB2):c.1655G>A (p.Ser552Asn)
NM_014795.4(ZEB2):c.1678C>T (p.Arg560Cys) rs730881194
NM_014795.4(ZEB2):c.1714A>C (p.Ile572Leu)
NM_014795.4(ZEB2):c.1722C>A (p.Asn574Lys)
NM_014795.4(ZEB2):c.1745C>T (p.Ser582Leu)
NM_014795.4(ZEB2):c.179C>T (p.Thr60Met) rs780890592
NM_014795.4(ZEB2):c.1877G>A (p.Gly626Glu) rs794727923
NM_014795.4(ZEB2):c.1879G>A (p.Val627Ile)
NM_014795.4(ZEB2):c.1885G>C (p.Val629Leu)
NM_014795.4(ZEB2):c.1947C>G (p.Ile649Met)
NM_014795.4(ZEB2):c.1975C>T (p.Leu659Phe) rs1560606673
NM_014795.4(ZEB2):c.199A>C (p.Asn67His)
NM_014795.4(ZEB2):c.2044G>C (p.Gly682Arg)
NM_014795.4(ZEB2):c.2050_2064del (p.Pro684_Val688del)
NM_014795.4(ZEB2):c.2124G>A (p.Leu708=)
NM_014795.4(ZEB2):c.2204C>G (p.Pro735Arg)
NM_014795.4(ZEB2):c.220G>A (p.Val74Met) rs767169568
NM_014795.4(ZEB2):c.2239C>T (p.Leu747Phe) rs1160664411
NM_014795.4(ZEB2):c.2275A>G (p.Arg759Gly)
NM_014795.4(ZEB2):c.2281A>T (p.Thr761Ser) rs867243713
NM_014795.4(ZEB2):c.2300C>T (p.Thr767Ile) rs755233964
NM_014795.4(ZEB2):c.2327A>G (p.Asp776Gly) rs1553961558
NM_014795.4(ZEB2):c.2337G>C (p.Arg779Ser) rs1573715809
NM_014795.4(ZEB2):c.2354C>G (p.Pro785Arg) rs1560606278
NM_014795.4(ZEB2):c.2390A>G (p.His797Arg) rs201227541
NM_014795.4(ZEB2):c.2418C>A (p.Phe806Leu) rs770951243
NM_014795.4(ZEB2):c.2419T>A (p.Ser807Thr)
NM_014795.4(ZEB2):c.2471T>C (p.Met824Thr) rs1553961536
NM_014795.4(ZEB2):c.2495C>A (p.Ala832Asp) rs730881179
NM_014795.4(ZEB2):c.2497A>G (p.Thr833Ala) rs1490526407
NM_014795.4(ZEB2):c.2541C>A (p.Asn847Lys) rs759097498
NM_014795.4(ZEB2):c.2545G>A (p.Val849Ile) rs1560606101
NM_014795.4(ZEB2):c.2619_2620delinsAT (p.Asn873_Asn874delinsLysTyr)
NM_014795.4(ZEB2):c.2621A>C (p.Asn874Thr) rs1477010525
NM_014795.4(ZEB2):c.2622T>A (p.Asn874Lys) rs745927130
NM_014795.4(ZEB2):c.2641A>C (p.Asn881His) rs794727922
NM_014795.4(ZEB2):c.2692C>T (p.Leu898Phe) rs1573715321
NM_014795.4(ZEB2):c.26G>A (p.Gly9Asp)
NM_014795.4(ZEB2):c.2707G>A (p.Ala903Thr)
NM_014795.4(ZEB2):c.2774G>A (p.Gly925Glu) rs1408659659
NM_014795.4(ZEB2):c.2847G>A (p.Met949Ile)
NM_014795.4(ZEB2):c.2855G>C (p.Arg952Thr) rs151256895
NM_014795.4(ZEB2):c.2869C>T (p.Arg957Trp) rs1354236085
NM_014795.4(ZEB2):c.2870G>A (p.Arg957Gln) rs371509136
NM_014795.4(ZEB2):c.2886+4A>C rs754532627
NM_014795.4(ZEB2):c.2935A>G (p.Met979Val)
NM_014795.4(ZEB2):c.2951C>T (p.Ser984Phe) rs143474223
NM_014795.4(ZEB2):c.295A>G (p.Asn99Asp) rs150665982
NM_014795.4(ZEB2):c.295_297AAC[1] (p.Asn100del) rs587776610
NM_014795.4(ZEB2):c.2967A>G (p.Lys989=)
NM_014795.4(ZEB2):c.2993T>C (p.Met998Thr)
NM_014795.4(ZEB2):c.29C>T (p.Pro10Leu)
NM_014795.4(ZEB2):c.3070A>G (p.Lys1024Glu) rs1573708232
NM_014795.4(ZEB2):c.3196C>T (p.His1066Tyr)
NM_014795.4(ZEB2):c.3202_3207del (p.Gly1068_Ser1069del) rs1553960777
NM_014795.4(ZEB2):c.3267A>C (p.Glu1089Asp) rs1553960775
NM_014795.4(ZEB2):c.3280G>A (p.Glu1094Lys)
NM_014795.4(ZEB2):c.3298C>T (p.His1100Tyr) rs1573707949
NM_014795.4(ZEB2):c.3308C>A (p.Pro1103His) rs1385679012
NM_014795.4(ZEB2):c.3357G>C (p.Gln1119His) rs1332911302
NM_014795.4(ZEB2):c.3408C>G (p.Ser1136Arg) rs1060500655
NM_014795.4(ZEB2):c.3430G>A (p.Gly1144Ser)
NM_014795.4(ZEB2):c.3451C>A (p.Leu1151Met) rs772764893
NM_014795.4(ZEB2):c.3512G>A (p.Ser1171Asn)
NM_014795.4(ZEB2):c.3527C>A (p.Pro1176His)
NM_014795.4(ZEB2):c.3538C>G (p.Arg1180Gly) rs756424812
NM_014795.4(ZEB2):c.3557G>T (p.Gly1186Val) rs748213160
NM_014795.4(ZEB2):c.3575A>C (p.Asp1192Ala) rs752093966
NM_014795.4(ZEB2):c.3599A>G (p.Glu1200Gly) rs1273805127
NM_014795.4(ZEB2):c.3610G>A (p.Asp1204Asn)
NM_014795.4(ZEB2):c.3640A>G (p.Met1214Val) rs199951665
NM_014795.4(ZEB2):c.364C>T (p.Pro122Ser) rs1573739706
NM_014795.4(ZEB2):c.385G>A (p.Ala129Thr) rs730881187
NM_014795.4(ZEB2):c.388A>G (p.Ile130Val) rs1057520175
NM_014795.4(ZEB2):c.430T>A (p.Phe144Ile) rs1057518371
NM_014795.4(ZEB2):c.466C>T (p.Arg156Cys) rs147021269
NM_014795.4(ZEB2):c.467G>A (p.Arg156His) rs1250217464
NM_014795.4(ZEB2):c.469G>A (p.Asp157Asn)
NM_014795.4(ZEB2):c.59C>T (p.Pro20Leu) rs730881206
NM_014795.4(ZEB2):c.703G>A (p.Glu235Lys) rs1553962069
NM_014795.4(ZEB2):c.73+6A>C rs756924190
NM_014795.4(ZEB2):c.751G>A (p.Ala251Thr) rs1437414345
NM_014795.4(ZEB2):c.757C>A (p.Arg253Ser)
NM_014795.4(ZEB2):c.785C>T (p.Thr262Ile)
NM_014795.4(ZEB2):c.797G>A (p.Gly266Glu) rs1057522361
NM_014795.4(ZEB2):c.905G>A (p.Arg302Gln) rs730881174
NM_014795.4(ZEB2):c.933G>T (p.Glu311Asp) rs1573717761

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