ClinVar Miner

Variants in gene SUFU 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
257 24 0 6 14 0 0 16

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 12 6
likely benign 12 0 6
benign 6 6 0

All variants with conflicting interpretations #

Total variants: 16
Download table as spreadsheet
HGVS dbSNP
NM_016169.3(SUFU):c.-33C>T rs201649559
NM_016169.3(SUFU):c.1018G>T (p.Ala340Ser) rs34135067
NM_016169.3(SUFU):c.1084C>T (p.Arg362Cys) rs36049457
NM_016169.3(SUFU):c.1245C>T (p.Gly415=) rs144158469
NM_016169.3(SUFU):c.1291T>C (p.Leu431=) rs141950577
NM_016169.3(SUFU):c.1299T>C (p.Ile433=) rs17114803
NM_016169.3(SUFU):c.12G>A (p.Leu4=) rs189234140
NM_016169.3(SUFU):c.1445C>T (p.Pro482Leu) rs765358771
NM_016169.3(SUFU):c.183-4delG rs1345403982
NM_016169.3(SUFU):c.210T>C (p.Tyr70=) rs35166585
NM_016169.3(SUFU):c.412G>A (p.Ala138Thr) rs34406289
NM_016169.3(SUFU):c.50C>T (p.Ala17Val) rs12780580
NM_016169.3(SUFU):c.528C>T (p.His176=) rs150569584
NM_016169.3(SUFU):c.600C>T (p.Ile200=) rs149513330
NM_016169.3(SUFU):c.839G>A (p.Arg280Gln) rs145704867
NM_016169.3(SUFU):c.910+14C>T rs202247757

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