ClinVar Miner

Variants in gene ZEB2 with conflicting interpretations

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Y axis minimum submission review status: Y axis collection method:
X axis minimum submission review status: X axis collection method:
Minimum conflict level:
Gene type:
ClinVar version:

If a variant has more than two submissions, it may have multiple conflicts and therefore be counted in more than one conflict column. If this is the case, the "Variants with any kind of conflict" cell will be less than the sum of the conflicted variants cells to its left.

Variants with only 1 submission per condition Variants with at least 2 submissions on the same condition and no conflicts Variants with a synonymous conflict
(e.g. benign vs non-pathogenic)
Variants with a confidence conflict
(e.g. benign vs likely benign)
Variants with a benign or likely benign vs uncertain conflict Variants with a category conflict
(e.g. benign vs affects)
Variants with a clinically significant conflict
(e.g. benign vs pathogenic)
Variants with any conflict
576 37 0 26 18 1 1 43

Significance breakdown #

In the table below, cells that correspond to a term paired with itself represent synonymous conflicts, i.e. variants that have been annotated with different terms that map to the same standard term. To compare the terms that were actually submitted, check the box in the filters section at the top of this page.

likely pathogenic uncertain significance likely benign benign drug response protective other
pathogenic 1 1 1 1 1 1 1
uncertain significance 0 0 16 5 0 0 0
likely benign 0 16 0 25 0 0 0
benign 0 5 25 0 0 0 0

All variants with conflicting interpretations #

Total variants: 43
Download table as spreadsheet
NM_014795.4(ZEB2):c.10C>G (p.Pro4Ala) rs146394306
NM_014795.4(ZEB2):c.1161A>G (p.Leu387=) rs146673563
NM_014795.4(ZEB2):c.1276T>A (p.Leu426Ile) rs201881288
NM_014795.4(ZEB2):c.1410T>A (p.Thr470=) rs34890427
NM_014795.4(ZEB2):c.1480C>T (p.Pro494Ser) rs144952836
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.1840C>T (p.Leu614=) rs145201706
NM_014795.4(ZEB2):c.1848T>G (p.Pro616=) rs144835963
NM_014795.4(ZEB2):c.1876G>A (p.Gly626Arg) rs727504224
NM_014795.4(ZEB2):c.2004G>T (p.Glu668Asp) rs767506087
NM_014795.4(ZEB2):c.2084G>A (p.Arg695Gln) rs147693839
NM_014795.4(ZEB2):c.2141C>T (p.Pro714Leu) rs112581563
NM_014795.4(ZEB2):c.2142G>A (p.Pro714=) rs201180901
NM_014795.4(ZEB2):c.219C>T (p.His73=) rs778851716
NM_014795.4(ZEB2):c.2206A>G (p.Met736Val) rs139191491
NM_014795.4(ZEB2):c.2226A>T (p.Pro742=) rs540345773
NM_014795.4(ZEB2):c.2230A>G (p.Ile744Val) rs112005830
NM_014795.4(ZEB2):c.2255C>T (p.Thr752Met) rs143438888
NM_014795.4(ZEB2):c.2361T>C (p.Asn787=) rs201567433
NM_014795.4(ZEB2):c.2601G>A (p.Lys867=) rs139369265
NM_014795.4(ZEB2):c.2766A>T (p.Pro922=) rs185223937
NM_014795.4(ZEB2):c.2855G>C (p.Arg952Thr) rs151256895
NM_014795.4(ZEB2):c.2886+4A>C rs754532627
NM_014795.4(ZEB2):c.2973C>T (p.Ile991=) rs572507342
NM_014795.4(ZEB2):c.304A>T (p.Ile102Phe) rs201109457
NM_014795.4(ZEB2):c.3067+6A>T rs143450927
NM_014795.4(ZEB2):c.3219C>T (p.His1073=) rs139944383
NM_014795.4(ZEB2):c.332-6C>T rs730881186
NM_014795.4(ZEB2):c.3640A>G (p.Met1214Val) rs199951665
NM_014795.4(ZEB2):c.374C>T (p.Thr125Met) rs727504227
NM_014795.4(ZEB2):c.403+18C>T rs116404871
NM_014795.4(ZEB2):c.462G>A (p.Glu154=) rs372940559
NM_014795.4(ZEB2):c.489C>T (p.Ile163=) rs138859323
NM_014795.4(ZEB2):c.759C>T (p.Arg253=) rs150853991
NM_014795.4(ZEB2):c.773G>A (p.Arg258Gln) rs730881173
NM_014795.4(ZEB2):c.798G>C (p.Gly266=) rs34961586
NM_014795.4(ZEB2):c.807+3G>C rs144925893
NM_014795.4(ZEB2):c.82_87del (p.Tyr28_Asp29del) rs730881214
NM_014795.4(ZEB2):c.917-21T>C rs35213774
NM_014795.4(ZEB2):c.9G>A (p.Gln3=) rs149882004
NM_014795.4(ZEB2):c.9G>C (p.Gln3His) rs149882004
Single allele

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