ClinVar Miner

Variants in gene SELENON 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
335 29 1 10 15 0 0 24

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 likely pathogenic uncertain significance likely benign benign
pathogenic 1 2 0 0 0
likely pathogenic 2 0 0 0 0
uncertain significance 0 0 0 13 4
likely benign 0 0 13 0 8
benign 0 0 4 8 0

All variants with conflicting interpretations #

Total variants: 24
Download table as spreadsheet
HGVS dbSNP
NM_020451.2(SELENON):c.-42T>C rs12121707
NM_020451.3(SELENON):c.-35T>C rs886038656
NM_020451.3(SELENON):c.1092+6C>G rs148071754
NM_020451.3(SELENON):c.1397G>A (p.Arg466Gln) rs121908185
NM_020451.3(SELENON):c.1500+7G>A rs200724231
NM_020451.3(SELENON):c.1501-31C>T rs72877469
NM_020451.3(SELENON):c.1596C>T (p.Gly532=) rs149623434
NM_020451.3(SELENON):c.1602+14C>T rs41284307
NM_020451.3(SELENON):c.1623C>T (p.Asn541=) rs199911454
NM_020451.3(SELENON):c.1638C>T (p.Ile546=) rs201066183
NM_020451.3(SELENON):c.1645G>A (p.Val549Met) rs147131452
NM_020451.3(SELENON):c.1654G>A (p.Glu552Lys) rs200128474
NM_020451.3(SELENON):c.1704G>A (p.Pro568=) rs754350384
NM_020451.3(SELENON):c.1710G>A (p.Thr570=) rs371398538
NM_020451.3(SELENON):c.409A>G (p.Thr137Ala) rs35019869
NM_020451.3(SELENON):c.427GAG[5] (p.Glu146dup) rs141295085
NM_020451.3(SELENON):c.465G>A (p.Thr155=) rs753774853
NM_020451.3(SELENON):c.550G>C (p.Ala184Pro) rs199742668
NM_020451.3(SELENON):c.583G>A (p.Ala195Thr) rs115852080
NM_020451.3(SELENON):c.729G>A (p.Pro243=) rs139020143
NM_020451.3(SELENON):c.732G>A (p.Pro244=) rs200765195
NM_020451.3(SELENON):c.747+39C>T rs114458946
NM_020451.3(SELENON):c.943G>A (p.Gly315Ser) rs121908188
NM_020451.3(SELENON):c.981C>T (p.Arg327=) rs147587542

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.