List of variants reported as benign for cardioencephalomyopathy, fatal infantile, due to cytochrome c oxidase deficiency 1 by Illumina Laboratory Services, Illumina

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Total variants: 8

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HGVS	dbSNP	gnomAD frequency
NM_005138.3(SCO2):c.633A>C (p.Ala211=)	rs12148	0.63421
NM_005138.3(SCO2):c.-78G>C	rs131806	0.51847
NM_001953.5(TYMP):c.1284T>A (p.Gly428=)	rs1138404	0.14075
NM_005138.3(SCO2):c.-18G>A	rs74479613	0.09346
NM_005138.3(SCO2):c.582C>T (p.Ser194=)	rs131811	0.05449
NM_005138.3(SCO2):c.327C>T (p.His109=)	rs75485962	0.02713
NM_005138.2(SCO2):c.-142G>C	rs145052206	0.01794
NM_005138.3(SCO2):c.59G>C (p.Arg20Pro)	rs140523

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