List of variants in gene COX20 reported as pathogenic for mitochondrial complex deficiency

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

Total variants: 5

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HGVS	dbSNP	gnomAD frequency
NM_198076.6(COX20):c.157+3G>C	rs367956888	0.00066
NM_198076.6(COX20):c.157+7A>G	rs1227651240	0.00001
NM_198076.6(COX20):c.222G>T (p.Trp74Cys)	rs766397584	0.00001
NM_198076.6(COX20):c.259C>T (p.Gln87Ter)	rs1680275439
NM_198076.6(COX20):c.98C>T (p.Ser33Leu)	rs1456182343

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