List of variants reported as benign for coenzyme Q10 deficiency by Illumina Laboratory Services, Illumina

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Total variants: 29

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HGVS	dbSNP	gnomAD frequency
NM_020312.4(COQ9):c.*490T>C	rs223870	0.97315
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.*464G>A	rs8159	0.31059
NM_020247.5(COQ8A):c.117G>A (p.Ala39=)	rs11549708	0.16388
NM_014317.5(PDSS1):c.*76C>T	rs12776877	0.13025
NM_020312.4(COQ9):c.*456C>A	rs223869	0.11358
NM_020247.5(COQ8A):c.*681G>A	rs10482	0.06118
NM_020247.5(COQ8A):c.255T>G (p.His85Gln)	rs2297411	0.04148
NM_020312.4(COQ9):c.102G>A (p.Pro34=)	rs223864	0.02864
NM_014317.5(PDSS1):c.89G>T (p.Gly30Val)	rs17855857	0.02444
NM_014317.5(PDSS1):c.*157T>G	rs1046187	0.02265
NM_020312.4(COQ9):c.*411C>T	rs112075830	0.01875
NM_020312.4(COQ9):c.864G>C (p.Lys288Asn)	rs61730662	0.01873
NM_020247.5(COQ8A):c.-10+8T>C	rs145688619	0.01402
NM_020247.5(COQ8A):c.993C>T (p.Phe331=)	rs41303129	0.01390
NM_020312.4(COQ9):c.921+13C>T	rs115677652	0.01317
NM_020247.5(COQ8A):c.63G>A (p.Ala21=)	rs11549709	0.01280
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.*727C>T	rs16846762	0.00659
NM_020247.5(COQ8A):c.655+9G>A	rs146526153	0.00658
NM_014317.5(PDSS1):c.407T>G (p.Phe136Cys)	rs77826284	0.00516
NM_014317.5(PDSS1):c.162+13A>G	rs12571799	0.00410
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.1440C>T (p.Phe480=)	rs12593

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