List of variants reported as pathogenic for mitochondrial complex deficiency by Juno Genomics, Hangzhou Juno Genomics, Inc

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Total variants: 4

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HGVS	dbSNP	gnomAD frequency
NM_198076.6(COX20):c.41A>G (p.Lys14Arg)	rs1057521790	0.00004
NM_001079866.2(BCS1L):c.245C>A (p.Ser82Ter)	rs749196764
NM_003172.4(SURF1):c.754_755del	rs782007828
NM_003172.4(SURF1):c.792_793del (p.Arg264fs)	rs782490558

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