ClinVar Miner

Variants in gene MOGS 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
76 11 0 8 8 0 0 13

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 8 3
likely benign 8 0 8
benign 3 8 0

All variants with conflicting interpretations #

Total variants: 13
Download table as spreadsheet
NM_006302.3(MOGS):c.12C>G (p.Gly4=) rs555329045
NM_006302.3(MOGS):c.1509A>C (p.Leu503=) rs759481390
NM_006302.3(MOGS):c.1587C>T (p.Asp529=) rs190772368
NM_006302.3(MOGS):c.1838G>A (p.Arg613Gln) rs142032474
NM_006302.3(MOGS):c.184G>A (p.Val62Met) rs79181168
NM_006302.3(MOGS):c.1944G>A (p.Glu648=) rs201547060
NM_006302.3(MOGS):c.2032C>T (p.Arg678Trp) rs13405869
NM_006302.3(MOGS):c.2055T>C (p.Tyr685=) rs202094225
NM_006302.3(MOGS):c.2353G>A (p.Gly785Ser) rs35533773
NM_006302.3(MOGS):c.249C>G (p.Ala83=) rs764778419
NM_006302.3(MOGS):c.499A>C (p.Arg167=) rs371747622
NM_006302.3(MOGS):c.85C>G (p.Arg29Gly) rs369653963
NM_006302.3(MOGS):c.881C>T (p.Pro294Leu) rs184209905

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