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 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
182 30 1 14 14 0 2 25

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 3 0 0 0
likely pathogenic 3 0 2 0 0
uncertain significance 0 2 0 11 8
likely benign 0 0 11 0 11
benign 0 0 8 11 0

All variants with conflicting interpretations #

Total variants: 25
Download table as spreadsheet
HGVS dbSNP
NM_020451.2(SELENON):c.-42T>C rs12121707
NM_020451.3(SELENON):c.1092+6C>G rs148071754
NM_020451.3(SELENON):c.1112G>A (p.Gly371Asp)
NM_020451.3(SELENON):c.1387+11C>T rs59653066
NM_020451.3(SELENON):c.1397G>A (p.Arg466Gln) rs121908185
NM_020451.3(SELENON):c.1427C>T (p.Ser476Leu) rs368377980
NM_020451.3(SELENON):c.1428G>A (p.Ser476=) rs41284305
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.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.409A>G (p.Thr137Ala) rs35019869
NM_020451.3(SELENON):c.427_429GAG[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.747+39C>T rs114458946
NM_020451.3(SELENON):c.846C>T (p.Ser282=) rs34177164
NM_020451.3(SELENON):c.852C>T (p.Phe284=) rs187880136
NM_020451.3(SELENON):c.872G>A (p.Arg291Gln) rs199564797
NM_020451.3(SELENON):c.943G>A (p.Gly315Ser) rs121908188
NM_020451.3(SELENON):c.981C>T (p.Arg327=) rs147587542

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