List of variants reported as likely benign for mitochondrial complex 4 deficiency, nuclear type 11 by Fulgent Genetics, Fulgent Genetics

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Total variants: 4

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HGVS	dbSNP	gnomAD frequency
NM_198076.6(COX20):c.222-3A>C	rs200065889	0.00003
NM_198076.6(COX20):c.115T>C (p.Leu39=)	rs1573315547
NM_198076.6(COX20):c.24T>C (p.Gly8=)	rs915488593
NM_198076.6(COX20):c.7G>T (p.Ala3Ser)	rs201152357

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