ClinVar Miner

Variants in gene TSEN2 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 17 1 6 7 0 1 13

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 uncertain significance likely benign benign
pathogenic 1 1 0 0
uncertain significance 1 0 7 1
likely benign 0 7 0 6
benign 0 1 6 0

All variants with conflicting interpretations #

Total variants: 13
Download table as spreadsheet
NM_025265.4(TSEN2):c.1029C>T (p.Tyr343=) rs371073764
NM_025265.4(TSEN2):c.1104A>G (p.Leu368=) rs761076607
NM_025265.4(TSEN2):c.1332A>G (p.Lys444=) rs113981920
NM_025265.4(TSEN2):c.272-4C>G rs41293385
NM_025265.4(TSEN2):c.389A>C (p.Lys130Thr) rs142211875
NM_025265.4(TSEN2):c.405G>A (p.Pro135=) rs140728375
NM_025265.4(TSEN2):c.522C>T (p.Asn174=) rs141580750
NM_025265.4(TSEN2):c.560G>C (p.Arg187Pro) rs146117200
NM_025265.4(TSEN2):c.66A>C (p.Pro22=) rs62637658
NM_025265.4(TSEN2):c.870A>G (p.Pro290=) rs542708828
NM_025265.4(TSEN2):c.926A>G (p.Tyr309Cys) rs113994149
NM_025265.4(TSEN2):c.961-14G>A rs748777382
NM_025265.4(TSEN2):c.990A>G (p.Lys330=) rs113260160

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