ClinVar Miner

Variants in gene ZNF335 with conflicting interpretations

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
96 7 0 8 12 0 0 20

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.

uncertain significance likely benign benign
uncertain significance 0 9 3
likely benign 9 0 8
benign 3 8 0

All variants with conflicting interpretations #

Total variants: 20
Download table as spreadsheet
HGVS dbSNP
NM_022095.4(ZNF335):c.1102+9T>C rs112458662
NM_022095.4(ZNF335):c.1830C>G (p.Leu610=) rs60180055
NM_022095.4(ZNF335):c.1963C>T (p.Pro655Ser) rs117132825
NM_022095.4(ZNF335):c.2185A>T (p.Ile729Phe) rs190178539
NM_022095.4(ZNF335):c.2280G>A (p.Gln760=) rs148186790
NM_022095.4(ZNF335):c.2821G>A (p.Ala941Thr) rs116247914
NM_022095.4(ZNF335):c.2961G>A (p.Gln987=) rs181061162
NM_022095.4(ZNF335):c.3180C>T (p.Pro1060=) rs61729182
NM_022095.4(ZNF335):c.3187C>A (p.Arg1063=) rs11905235
NM_022095.4(ZNF335):c.3392G>A (p.Arg1131Lys) rs114864530
NM_022095.4(ZNF335):c.3445A>G (p.Ile1149Val) rs143113106
NM_022095.4(ZNF335):c.3639C>T (p.Thr1213=) rs191074858
NM_022095.4(ZNF335):c.3720A>G (p.Glu1240=) rs763575505
NM_022095.4(ZNF335):c.3820-7_3820-6del rs150750750
NM_022095.4(ZNF335):c.3843A>G (p.Pro1281=) rs35291173
NM_022095.4(ZNF335):c.642C>T (p.Ser214=) rs3848719
NM_022095.4(ZNF335):c.648G>A (p.Pro216=) rs201180565
NM_022095.4(ZNF335):c.808C>T (p.Arg270Cys) rs145110365
NM_022095.4(ZNF335):c.825C>T (p.Ala275=) rs797046125
NM_022095.4(ZNF335):c.826G>A (p.Ala276Thr) rs117802609

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