ClinVar Miner

Variants in gene IL17RA 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
443 28 0 1 21 0 0 22

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.

uncertain significance likely benign benign
uncertain significance 0 19 2
likely benign 19 0 1
benign 2 1 0

All variants with conflicting interpretations #

Total variants: 22
Download table as spreadsheet
NM_014339.6(IL17RA):c.1045+6C>T rs763664351
NM_014339.6(IL17RA):c.1045+7G>A rs572837622
NM_014339.6(IL17RA):c.1046G>C (p.Gly349Ala) rs143897670
NM_014339.6(IL17RA):c.1174G>T (p.Val392Leu) rs146478431
NM_014339.6(IL17RA):c.1407C>T (p.Cys469=) rs41396346
NM_014339.6(IL17RA):c.1493C>T (p.Thr498Ile) rs41529049
NM_014339.6(IL17RA):c.152C>T (p.Thr51Met) rs143008696
NM_014339.6(IL17RA):c.1632G>C (p.Pro544=) rs550947413
NM_014339.6(IL17RA):c.1689C>T (p.Gly563=) rs146292661
NM_014339.6(IL17RA):c.1728C>T (p.Asp576=) rs767714232
NM_014339.6(IL17RA):c.2466G>A (p.Gly822=) rs373070776
NM_014339.6(IL17RA):c.36G>T (p.Pro12=) rs886057200
NM_014339.6(IL17RA):c.465G>C (p.Gln155His) rs142199303
NM_014339.6(IL17RA):c.676G>C (p.Glu226Gln) rs144085995
NM_014339.6(IL17RA):c.894C>T (p.Ser298=) rs374537654
NM_014339.6(IL17RA):c.958T>C (p.Trp320Arg) rs140221307
NM_014339.7(IL17RA):c.1232C>T (p.Ala411Val) rs151166583
NM_014339.7(IL17RA):c.1381C>T (p.Arg461Trp) rs554211497
NM_014339.7(IL17RA):c.1475G>A (p.Arg492Lys)
NM_014339.7(IL17RA):c.30T>A (p.Ala10=) rs577217331
NM_014339.7(IL17RA):c.641C>T (p.Ala214Val) rs558799480
NM_014339.7(IL17RA):c.978G>A (p.Thr326=) rs143239201

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.