Variants from Genetic Diagnostics Department, Viafet Genomics Laboratory with conflicting interpretations

Minimum review status of the submission from Genetic Diagnostics Department, Viafet Genomics Laboratory:	★☆☆☆ criteria provided ★★★☆ reviewed by expert panel ★★★★ practice guideline	Collection method of the submission from Genetic Diagnostics Department, Viafet Genomics Laboratory:	clinical testing curation literature only research other
Minimum review status of the other submission:	★☆☆☆ criteria provided ★★★☆ reviewed by expert panel ★★★★ practice guideline	Collection method of the other submission:	clinical testing curation literature only research other
Minimum conflict level: confidence conflict (e.g. benign vs likely benign) benign or likely benign vs uncertain conflict category conflict (e.g. benign vs affects) clinically significant conflict (e.g. benign vs pathogenic) Report conflict between different conditions
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version: 2024-06-30

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
8	5	1	5	0	0	3	9

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
Genetic Diagnostics Department, Viafet Genomics Laboratory		pathogenic	likely pathogenic	uncertain significance
	pathogenic	1	2	3
	likely pathogenic	3	0	0

Submitter to submitter summary #

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
Invitae	0	3	0	2	0	0	0	2
Center for Genomic Medicine, King Faisal Specialist Hospital and Research Center	0	1	0	0	0	0	2	2
Baylor Genetics	0	2	0	1	0	0	0	1
Revvity Omics, Revvity	0	2	0	1	0	0	0	1
GeneReviews	0	3	1	0	0	0	0	1
Institute of Human Genetics, University of Leipzig Medical Center	0	0	0	0	0	0	1	1
Myriad Genetics, Inc.	0	2	0	1	0	0	0	1

All variants with conflicting interpretations #

HGVS	dbSNP	gnomAD frequency
NM_000250.2(MPO):c.1705C>T (p.Arg569Trp)	rs119468010	0.00173
NM_002772.3(TMPRSS15):c.2135C>G (p.Ser712Ter)	rs77200626	0.00064
NM_000157.4(GBA1):c.1342G>C (p.Asp448His)	rs1064651	0.00020
NM_207352.4(CYP4V2):c.332T>C (p.Ile111Thr)	rs119103283	0.00005
NM_001083116.3(PRF1):c.1122G>A (p.Trp374Ter)	rs104894176	0.00003
NM_004004.6(GJB2):c.506G>A (p.Cys169Tyr)	rs774518779	0.00001
NM_000046.5(ARSB):c.898+1G>A	rs1751669303
NM_000137.4(FAH):c.328C>T (p.Gln110Ter)	rs754444882
NM_001130987.2(DYSF):c.1762C>T (p.Gln588Ter)	rs886042633