ClinVar Miner

Variants in gene TRIOBP 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
207 36 0 27 13 0 1 38

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 1 0 0
uncertain significance 1 0 11 5
likely benign 0 11 0 27
benign 0 5 27 0

All variants with conflicting interpretations #

Total variants: 38
Download table as spreadsheet
HGVS dbSNP
NM_001039141.3(TRIOBP):c.1478G>A (p.Ser493Asn) rs4821700
NM_001039141.3(TRIOBP):c.265C>G (p.Pro89Ala) rs199646135
NM_001039141.3(TRIOBP):c.3232C>T (p.Arg1078Cys) rs200359708
NM_001039141.3(TRIOBP):c.3309C>T (p.His1103=) rs199594270
NM_001039141.3(TRIOBP):c.363C>A (p.Ser121=) rs201843208
NM_001039141.3(TRIOBP):c.391G>A (p.Gly131Ser) rs144634857
NM_001039141.3(TRIOBP):c.3954C>T (p.Ser1318=) rs200990219
NM_001039141.3(TRIOBP):c.4031G>A (p.Arg1344Gln) rs34066624
NM_001039141.3(TRIOBP):c.4077T>C (p.Pro1359=) rs139074745
NM_001039141.3(TRIOBP):c.4165C>A (p.Leu1389Ile) rs144175566
NM_001039141.3(TRIOBP):c.4178C>T (p.Pro1393Leu) rs28450766
NM_001039141.3(TRIOBP):c.4703C>G (p.Ala1568Gly) rs569914227
NM_001039141.3(TRIOBP):c.4726C>T (p.Arg1576Cys) rs200113910
NM_001039141.3(TRIOBP):c.4728T>C (p.Arg1576=) rs112874177
NM_001039141.3(TRIOBP):c.4783C>T (p.Arg1595Cys) rs201117318
NM_001039141.3(TRIOBP):c.483G>A (p.Glu161=) rs368119524
NM_001039141.3(TRIOBP):c.5014G>T (p.Gly1672Ter) rs200045032
NM_001039141.3(TRIOBP):c.5052G>T (p.Thr1684=) rs41283241
NM_001039141.3(TRIOBP):c.5058C>G (p.Pro1686=) rs113459040
NM_001039141.3(TRIOBP):c.5588C>T (p.Ala1863Val) rs140528529
NM_001039141.3(TRIOBP):c.5764C>T (p.Arg1922Trp) rs183941928
NM_001039141.3(TRIOBP):c.584C>T (p.Thr195Ile) rs143157673
NM_001039141.3(TRIOBP):c.5853G>A (p.Leu1951=) rs55821172
NM_001039141.3(TRIOBP):c.6135C>T (p.Pro2045=) rs11546529
NM_001039141.3(TRIOBP):c.634G>A (p.Gly212Ser) rs201794404
NM_001039141.3(TRIOBP):c.6360C>T (p.Ser2120=) rs375936342
NM_001039141.3(TRIOBP):c.6362C>T (p.Ser2121Leu) rs201724032
NM_001039141.3(TRIOBP):c.6414G>A (p.Gln2138=) rs369245613
NM_001039141.3(TRIOBP):c.6472+10C>T rs369182277
NM_001039141.3(TRIOBP):c.6472+14G>T rs45503898
NM_001039141.3(TRIOBP):c.6571C>T (p.His2191Tyr) rs61729063
NM_001039141.3(TRIOBP):c.6736G>A (p.Glu2246Lys) rs138139146
NM_001039141.3(TRIOBP):c.6741G>A (p.Leu2247=) rs375013523
NM_001039141.3(TRIOBP):c.6771G>A (p.Gln2257=) rs200793989
NM_001039141.3(TRIOBP):c.6806A>G (p.Asn2269Ser) rs61729060
NM_001039141.3(TRIOBP):c.6899T>C (p.Val2300Ala) rs61737841
NM_001039141.3(TRIOBP):c.7010G>A (p.Arg2337Gln) rs200850285
NM_001039141.3(TRIOBP):c.7032G>A (p.Glu2344=) rs61737839

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