List of variants in gene COQ7 reported as benign by GeneDx

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 15

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HGVS	dbSNP	gnomAD frequency
NM_016138.5(COQ7):c.577-305G>A	rs11074360	0.92326
NM_016138.5(COQ7):c.74-29A>G	rs4782202	0.91633
NM_016138.5(COQ7):c.368-278_368-275dup	rs56155740	0.89145
NM_016138.5(COQ7):c.308C>T (p.Thr103Met)	rs11074359	0.55635
NM_016138.5(COQ7):c.252+121C>T	rs9673167	0.54614
NM_016138.5(COQ7):c.74-215G>A	rs12443533	0.48336
NM_016138.5(COQ7):c.252+186A>G	rs56267950	0.05247
NM_016138.5(COQ7):c.507+240A>G	rs58113237	0.04260
NM_016138.5(COQ7):c.367+4C>T	rs114401101	0.01413
NM_016138.5(COQ7):c.234C>T (p.Ser78=)	rs11859129	0.01375
NM_016138.5(COQ7):c.124G>C (p.Asp42His)	rs138730205	0.00671
NM_016138.5(COQ7):c.545A>G (p.His182Arg)	rs139931303	0.00173
NM_016138.5(COQ7):c.*143dup	rs34110874
NM_016138.5(COQ7):c.*82C>G	rs8051232
NM_016138.5(COQ7):c.577-287G>A	rs116445775

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