ClinVar Miner

Variants in gene WWOX 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 Variants with at least 2 submissions 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 kind of conflict
192 35 0 10 6 0 4 19

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.

pathogenic likely pathogenic uncertain significance likely benign benign
pathogenic 0 2 1 0 1
likely pathogenic 2 0 2 0 0
uncertain significance 1 2 0 3 4
likely benign 0 0 3 0 8
benign 1 0 4 8 0

All variants with conflicting interpretations #

Total variants: 19
Download table as spreadsheet
HGVS dbSNP
NM_016373.3(WWOX):c.332C>G (p.Thr111Ser) rs114755364
NM_016373.3(WWOX):c.358C>T (p.Arg120Trp) rs141361080
NM_016373.3(WWOX):c.410G>A (p.Gly137Glu) rs761879076
NM_016373.3(WWOX):c.421G>A (p.Ala141Thr) rs369907002
NM_016373.3(WWOX):c.468G>T (p.Arg156Ser) rs140817689
NM_016373.3(WWOX):c.517-10C>G rs199820033
NM_016373.3(WWOX):c.605+5G>A rs1039151413
NM_016373.3(WWOX):c.613C>A (p.His205Asn) rs74860463
NM_016373.3(WWOX):c.618G>A (p.Val206=) rs376279847
NM_016373.3(WWOX):c.749C>G (p.Ser250Ter) rs368928190
NM_016373.3(WWOX):c.754C>G (p.Pro252Ala) rs75559202
NM_016373.3(WWOX):c.807C>T (p.Asn269=) rs62034095
NM_016373.3(WWOX):c.816G>T (p.Leu272Phe) rs186745328
NM_016373.3(WWOX):c.835C>T (p.Arg279Cys) rs77314072
NM_016373.3(WWOX):c.876T>G (p.Ala292=) rs74030232
NM_016373.3(WWOX):c.885G>A (p.Arg295=) rs79771882
NM_016373.3(WWOX):c.990C>G (p.Asn330Lys) rs117209694
NM_016373.4(WWOX):c.583G>T (p.Glu195Ter)
NM_130791.3(WWOX):c.544A>G (p.Lys182Glu) rs77067228

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