List of variants in gene combination NCAPH2, SCO2, TYMP reported as benign for Cardioencephalomyopathy, fatal infantile, due to cytochrome c oxidase deficiency 1

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
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Total variants: 4

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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.582C>T (p.Ser194=)	rs131811	0.05449
NM_005138.3(SCO2):c.327C>T (p.His109=)	rs75485962	0.02713
NM_005138.3(SCO2):c.59G>C (p.Arg20Pro)	rs140523

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