List of variants in gene combination COQ2, LOC112997540 reported by PreventionGenetics, part of Exact Sciences

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 15

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HGVS	dbSNP	gnomAD frequency
NM_001358921.2(COQ2):c.46G>T (p.Val16Leu)	rs6818847	0.62431
NM_001358921.2(COQ2):c.189G>T (p.Val63=)	rs368507578	0.00719
NM_001358921.2(COQ2):c.194A>C (p.Asp65Ala)	rs375934957	0.00574
NM_015697.9(COQ2):c.30G>A (p.Arg10_Lys11=)	rs183012002	0.00375
NM_001358921.2(COQ2):c.137C>T (p.Pro46Leu)	rs566165293	0.00193
NM_001358921.2(COQ2):c.170G>C (p.Ser57Thr)	rs550949678	0.00102
NM_001358921.2(COQ2):c.136C>T (p.Pro46Ser)	rs767013819	0.00029
NM_015697.9(COQ2):c.61G>A (p.Gly21Ser)	rs766552045	0.00002
NM_001358921.2(COQ2):c.-30del	rs1418018696
NM_001358921.2(COQ2):c.219G>T (p.Pro73=)
NM_001358921.2(COQ2):c.27C>T (p.Phe9=)
NM_001358921.2(COQ2):c.2T>C (p.Met1Thr)
NM_001358921.2(COQ2):c.99T>A (p.Arg33=)
NM_015697.9(COQ2):c.64A>C (p.Arg22=)	rs112033303
NM_015697.9(COQ2):c.64A>T (p.Arg22Ter)	rs112033303

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