ClinVar Miner

Variants in gene DAG1 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
171 37 0 7 13 0 1 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 uncertain significance likely benign benign
pathogenic 0 0 0 1
uncertain significance 0 0 13 2
likely benign 0 13 0 7
benign 1 2 7 0

All variants with conflicting interpretations #

Total variants: 19
Download table as spreadsheet
NM_001165928.3(DAG1):c.1212G>A (p.Thr404=) rs139781017
NM_001165928.3(DAG1):c.1233G>A (p.Val411=) rs145765079
NM_001165928.3(DAG1):c.1308G>A (p.Thr436=) rs143763229
NM_001165928.3(DAG1):c.1719C>T (p.His573=) rs146157416
NM_001165928.3(DAG1):c.1773C>T (p.Phe591=) rs2229010
NM_001165928.3(DAG1):c.2082C>T (p.Asn694=) rs146453412
NM_001165928.3(DAG1):c.222C>T (p.Val74=)
NM_001165928.3(DAG1):c.2256C>T (p.His752=) rs1801143
NM_001165928.3(DAG1):c.2313C>T (p.Ala771=) rs764289801
NM_001165928.3(DAG1):c.2520T>C (p.Thr840=) rs149564053
NM_001165928.3(DAG1):c.258G>C (p.Leu86Phe) rs145403829
NM_001165928.3(DAG1):c.259A>G (p.Ile87Val) rs116717961
NM_001165928.3(DAG1):c.278T>C (p.Ile93Thr) rs149218670
NM_001165928.3(DAG1):c.331G>A (p.Asp111Asn) rs117209107
NM_001165928.3(DAG1):c.384G>A (p.Val128=) rs143829263
NM_001165928.3(DAG1):c.384G>T (p.Val128=) rs143829263
NM_001165928.3(DAG1):c.498G>A (p.Ser166=) rs794727500
NM_001165928.3(DAG1):c.599C>G (p.Thr200Ser) rs41290704
NM_001165928.3(DAG1):c.927C>T (p.Arg309=) rs551679833

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