ClinVar Miner

Variants in gene IL10RA with conflicting interpretations

See also:
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
141 24 0 9 8 0 1 17

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.

likely pathogenic uncertain significance likely benign benign
likely pathogenic 0 1 0 0
uncertain significance 1 0 5 4
likely benign 0 5 0 9
benign 0 4 9 0

All variants with conflicting interpretations #

Total variants: 17
Download table as spreadsheet
NM_001558.3(IL10RA):c.67+8T>C rs200992970
NM_001558.3(IL10RA):c.810+10G>A rs12290349
NM_001558.4(IL10RA):c.1188G>A (p.Arg396=) rs35465632
NM_001558.4(IL10RA):c.1360G>A (p.Glu454Lys) rs79887053
NM_001558.4(IL10RA):c.1401G>A (p.Ser467=) rs150551465
NM_001558.4(IL10RA):c.144C>T (p.Ile48=) rs140466541
NM_001558.4(IL10RA):c.1539G>A (p.Thr513=) rs372503247
NM_001558.4(IL10RA):c.170A>G (p.Tyr57Cys) rs201643277
NM_001558.4(IL10RA):c.181C>G (p.Leu61Val) rs4252250
NM_001558.4(IL10RA):c.337G>A (p.Val113Ile) rs4252303
NM_001558.4(IL10RA):c.696C>T (p.Thr232=) rs4252311
NM_001558.4(IL10RA):c.698T>G (p.Val233Gly) rs138929400
NM_001558.4(IL10RA):c.716T>C (p.Phe239Ser) rs541386535
NM_001558.4(IL10RA):c.72A>C (p.Thr24=) rs560128585
NM_001558.4(IL10RA):c.781C>T (p.Arg261Trp) rs201396764
NM_001558.4(IL10RA):c.931T>C (p.Leu311=) rs148808529
NM_001558.4(IL10RA):c.96G>A (p.Val32=) rs377525753

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.