ClinVar Miner

Variants in gene TK2 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 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
106 6 12 9 1 0 3 21

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 12 3 3 0 0
likely pathogenic 3 0 0 0 0
uncertain significance 3 0 0 1 1
likely benign 0 0 1 0 6
benign 0 0 1 6 0

All variants with conflicting interpretations #

Total variants: 21
Download table as spreadsheet
NM_004614.5(TK2):c.122C>A (p.Pro41His) rs201904720
NM_004614.5(TK2):c.156+15T>C rs80083556
NM_004614.5(TK2):c.156+2T>C rs281865499
NM_004614.5(TK2):c.157-12G>A rs117229729
NM_004614.5(TK2):c.159C>G (p.Ile53Met) rs137854432
NM_004614.5(TK2):c.173A>G (p.Asn58Ser) rs138439950
NM_004614.5(TK2):c.191C>T (p.Thr64Met) rs281865487
NM_004614.5(TK2):c.231+10C>T rs187517309
NM_004614.5(TK2):c.268C>T (p.Arg90Cys) rs281865489
NM_004614.5(TK2):c.323C>T (p.Thr108Met) rs137854431
NM_004614.5(TK2):c.361C>A (p.His121Asn) rs137854429
NM_004614.5(TK2):c.416C>T (p.Ala139Val) rs281865494
NM_004614.5(TK2):c.547C>G (p.Arg183Gly) rs137886900
NM_004614.5(TK2):c.547C>T (p.Arg183Trp) rs137886900
NM_004614.5(TK2):c.562A>G (p.Thr188Ala) rs281865495
NM_004614.5(TK2):c.575G>A (p.Arg192Lys) rs281865496
NM_004614.5(TK2):c.604_606del (p.Lys202del) rs281865501
NM_004614.5(TK2):c.635T>A (p.Ile212Asn) rs137854430
NM_004614.5(TK2):c.700-13G>A rs16956600
NM_004614.5(TK2):c.760C>T (p.Arg254Ter) rs281865498
NM_004614.5(TK2):c.94C>T (p.Arg32Trp) rs200121712

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