ClinVar Miner

Variants in gene TG 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
145 7 0 9 2 3 3 14

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 risk factor
pathogenic 0 3 0 0 0
uncertain significance 3 0 1 1 0
likely benign 0 1 0 9 3
benign 0 1 9 0 3
risk factor 0 0 3 3 0

All variants with conflicting interpretations #

Total variants: 14
Download table as spreadsheet
NM_003235.5(TG):c.1543C>G (p.Gln515Glu) rs180222
NM_003235.5(TG):c.2200T>G (p.Ser734Ala) rs180223
NM_003235.5(TG):c.229G>A (p.Gly77Ser) rs142698837
NM_003235.5(TG):c.2334T>C (p.Pro778=) rs2069550
NM_003235.5(TG):c.3082A>G (p.Met1028Val) rs853326
NM_003235.5(TG):c.3935A>G (p.Asp1312Gly) rs2069556
NM_003235.5(TG):c.4506T>C (p.Ala1502=) rs853304
NM_003235.5(TG):c.4527C>T (p.His1509=) rs201216611
NM_003235.5(TG):c.5512G>A (p.Asp1838Asn) rs2069561
NM_003235.5(TG):c.5921T>C (p.Met1974Thr) rs56230101
NM_003235.5(TG):c.5995C>T (p.Arg1999Trp) rs2076740
NM_003235.5(TG):c.6379C>T (p.Arg2127Ter) rs375424292
NM_003235.5(TG):c.638+5G>A rs774274702
NM_003235.5(TG):c.7920C>T (p.Tyr2640=) rs2294024

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