Variants with conflicting interpretations studied for Peroxisome biogenesis disorder 9B

Minimum review status of the submission for Peroxisome biogenesis disorder 9B:		Collection method of the submission for Peroxisome biogenesis disorder 9B:
Minimum review status of the other submission:		Collection method of the other submission:
Minimum conflict level: Report conflict between different conditions
Show significances as they were submitted (without aggregation into standard terms)
		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
499	28	0	6	10	0	2	18

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 conditions
Peroxisome biogenesis disorder 9B		pathogenic	likely pathogenic	uncertain significance	likely benign	benign
	pathogenic	0	4	0	0	0
	likely pathogenic	4	0	2	0	0
	uncertain significance	0	2	0	7	3
	likely benign	0	0	7	0	2
	benign	0	0	3	2	0

Condition to condition summary #

Total conditions: 1

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Condition	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
Peroxisome biogenesis disorder 9B	499	28	0	6	10	0	2	18

All variants with conflicting interpretations #

Total variants: 18

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HGVS	dbSNP	gnomAD frequency
NM_000288.4(PEX7):c.377A>C (p.Gln126Pro)	rs113268723	0.00376
NM_000288.4(PEX7):c.615C>T (p.Asp205=)	rs147298444	0.00085
NM_000288.4(PEX7):c.418-4G>T	rs199552223	0.00054
NM_000288.4(PEX7):c.94C>T (p.Leu32=)	rs886061118	0.00032
NM_000288.4(PEX7):c.695G>A (p.Arg232Gln)	rs191969418	0.00011
NM_000288.4(PEX7):c.340-10A>G	rs267608255	0.00006
NM_000288.4(PEX7):c.804-5C>T	rs369653173	0.00004
NM_000288.4(PEX7):c.576C>T (p.Ile192=)	rs776411851	0.00003
NM_000288.4(PEX7):c.903+8A>G	rs779919482	0.00003
NM_000288.4(PEX7):c.748-10T>C	rs886061122	0.00001
NM_000288.4(PEX7):c.843A>G (p.Thr281=)	rs767903764	0.00001
NM_000288.4(PEX7):c.130+11G>T	rs886061119
NM_000288.4(PEX7):c.130+13C>A	rs886061120
NM_000288.4(PEX7):c.277C>T (p.Gln93Ter)	rs763514968
NM_000288.4(PEX7):c.488G>A (p.Trp163Ter)	rs1173171051
NM_000288.4(PEX7):c.549G>A (p.Trp183Ter)
NM_000288.4(PEX7):c.74C>T (p.Ser25Phe)	rs61753236
NM_000288.4(PEX7):c.870_871insCAA (p.Cys290_Gly291insGln)	rs267608257

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