List of variants in gene COQ8B reported as uncertain significance by Mayo Clinic Laboratories, Mayo Clinic

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: 5

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HGVS	dbSNP	gnomAD frequency
NM_024876.4(COQ8B):c.187C>T (p.Arg63Trp)	rs113358395	0.00351
NM_024876.4(COQ8B):c.1364A>G (p.Tyr455Cys)	rs144343899	0.00024
NM_024876.4(COQ8B):c.872C>T (p.Ala291Val)	rs138255798	0.00019
NM_024876.4(COQ8B):c.520_521inv (p.His174Cys)
NM_024876.4(COQ8B):c.695C>T (p.Thr232Met)	rs370082401

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