ClinVar Miner

Variants from Department of Ophthalmology, Flinders University with conflicting interpretations

Location: Australia  Primary collection method: clinical testing
Minimum review status of the submission from Department of Ophthalmology, Flinders University: Collection method of the submission from Department of Ophthalmology, Flinders University:
Minimum review status of the other submission: Collection method of the other submission:
Minimum conflict level:
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
11 1 0 2 0 0 3 5

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.

All submitters
Department of Ophthalmology, Flinders University pathogenic likely pathogenic uncertain significance likely benign
pathogenic 0 1 1 1
likely pathogenic 1 0 1 1

Submitter to submitter summary #

Total submitters: 5
Download table as spreadsheet
Submitter 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
GeneDx 0 0 0 1 0 0 1 2
PreventionGenetics, part of Exact Sciences 0 1 0 1 0 0 1 2
Department of Pathology and Laboratory Medicine, Sinai Health System 0 0 0 0 0 0 1 1
Breda Genetics srl 0 0 0 0 0 0 1 1
Dept. Genetics and Cancer, Menzies Institute for Medical Research, University of Tasmania 0 0 0 1 0 0 0 1

All variants with conflicting interpretations #

Total variants: 5
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_014617.4(CRYGA):c.239G>A (p.Arg80His) rs139353014 0.00221
NM_015480.3(NECTIN3):c.886A>C (p.Asn296His) rs79006549 0.00178
NM_000496.3(CRYBB2):c.463C>T (p.Gln155Ter) rs74315489 0.00001
NM_000394.4(CRYAA):c.440del (p.Gln147fs) rs1114167311
NM_021954.4(GJA3):c.56C>T (p.Thr19Met) rs1114167307

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