List of variants reported as uncertain significance for Cardioencephalomyopathy, fatal infantile, due to cytochrome c oxidase deficiency 1; Myopia 6 by Fulgent Genetics, Fulgent Genetics

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Total variants: 8

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HGVS	dbSNP	gnomAD frequency
NM_005138.3(SCO2):c.713C>T (p.Thr238Met)	rs149439760	0.00039
NM_005138.3(SCO2):c.378G>A (p.Met126Ile)	rs150880212	0.00025
NM_005138.3(SCO2):c.127C>G (p.Pro43Ala)	rs147185850	0.00022
NM_005138.3(SCO2):c.784C>T (p.Arg262Cys)	rs201174948	0.00009
NM_005138.3(SCO2):c.244A>G (p.Lys82Glu)	rs765425160	0.00003
NM_005138.3(SCO2):c.616C>T (p.Arg206Cys)	rs748770403	0.00003
NM_005138.3(SCO2):c.508G>C (p.Glu170Gln)	rs753614511
NM_005138.3(SCO2):c.652dup (p.Gln218fs)	rs2148670938

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