List of variants in gene COQ8A reported as benign for not specified

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: 34

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HGVS	dbSNP	gnomAD frequency
NM_020247.5(COQ8A):c.1660-9T>C	rs7552783	0.45219
NM_020247.5(COQ8A):c.1716T>C (p.Ser572=)	rs3738725	0.42035
NM_020247.5(COQ8A):c.1573-20C>G	rs2297416	0.38143
NM_020247.5(COQ8A):c.117G>A (p.Ala39=)	rs11549708	0.16388
NM_020247.5(COQ8A):c.255T>G (p.His85Gln)	rs2297411	0.04148
NM_020247.5(COQ8A):c.993C>T (p.Phe331=)	rs41303129	0.01390
NM_020247.5(COQ8A):c.63G>A (p.Ala21=)	rs11549709	0.01280
NM_020247.5(COQ8A):c.1053C>T (p.Gly351=)	rs55958233	0.01103
NM_020247.5(COQ8A):c.655+9G>A	rs146526153	0.00658
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.948C>T (p.Leu316=)	rs55637780	0.00229
NM_020247.5(COQ8A):c.618G>A (p.Val206=)	rs115855910	0.00220
NM_020247.5(COQ8A):c.78C>T (p.His26=)	rs150541057	0.00214
NM_020247.5(COQ8A):c.298G>T (p.Asp100Tyr)	rs150696959	0.00153
NM_020247.5(COQ8A):c.1824C>T (p.Ser608=)	rs141270350	0.00152
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.1876C>T (p.Arg626Cys)	rs141725964	0.00089
NM_020247.5(COQ8A):c.1797C>T (p.Leu599=)	rs139551241	0.00070
NM_020247.5(COQ8A):c.67G>A (p.Val23Met)	rs35582308	0.00058
NM_020247.5(COQ8A):c.258A>C (p.Ala86=)	rs137872711	0.00043
NM_020247.5(COQ8A):c.1399-13G>A	rs73087649	0.00041
NM_020247.5(COQ8A):c.1089C>T (p.Gly363=)	rs139570869	0.00034
NM_020247.5(COQ8A):c.1188C>T (p.Asp396=)	rs139133094	0.00026
NM_020247.5(COQ8A):c.1572+7G>A	rs371874740	0.00014
NM_020247.5(COQ8A):c.1644C>T (p.Thr548=)	rs141423403	0.00013
NM_020247.5(COQ8A):c.1011C>T (p.Ala337=)	rs36006006	0.00011
NM_020247.5(COQ8A):c.731-9C>T	rs367603340	0.00002
NM_020247.5(COQ8A):c.1399-12C>T	rs377529632	0.00001
NM_020247.5(COQ8A):c.909C>T (p.Ser303=)	rs202036077	0.00001
NM_020247.5(COQ8A):c.1020C>A (p.Ser340=)	rs181558991
NM_020247.5(COQ8A):c.1440C>T (p.Phe480=)	rs12593

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