List of variants in gene COQ8A reported as likely benign by Illumina Laboratory Services, Illumina

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: 13

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HGVS	dbSNP	gnomAD frequency
NM_020247.5(COQ8A):c.*681G>A	rs10482	0.06118
NM_020247.5(COQ8A):c.255T>G (p.His85Gln)	rs2297411	0.04148
NM_020247.5(COQ8A):c.*133G>A	rs149820067	0.01173
NM_020247.5(COQ8A):c.1053C>T (p.Gly351=)	rs55958233	0.01103
NM_020247.5(COQ8A):c.*790A>G	rs12565212	0.00855
NM_020247.5(COQ8A):c.291C>T (p.Ser97=)	rs111529228	0.00567
NM_020247.5(COQ8A):c.1185C>T (p.Ile395=)	rs17849927	0.00488
NM_020247.5(COQ8A):c.384C>T (p.Ala128=)	rs139970507	0.00250
NM_020247.5(COQ8A):c.298G>T (p.Asp100Tyr)	rs150696959	0.00153
NM_020247.5(COQ8A):c.*230G>A	rs117808661	0.00143
NM_020247.5(COQ8A):c.1914C>T (p.Ser638=)	rs56043893	0.00141
NM_020247.5(COQ8A):c.238C>T (p.His80Tyr)	rs76249490	0.00140
NM_020247.5(COQ8A):c.*761G>A	rs145779574

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