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

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Total variants: 5

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HGVS	dbSNP	gnomAD frequency
NM_005138.3(SCO2):c.512G>A (p.Arg171Gln)	rs775173963	0.00002
NM_005138.3(SCO2):c.535C>T (p.Arg179Cys)	rs780314255	0.00001
NM_005138.3(SCO2):c.202G>C (p.Gly68Arg)
NM_005138.3(SCO2):c.221C>A (p.Ala74Asp)
NM_005138.3(SCO2):c.386G>A (p.Gly129Asp)

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