List of variants in gene COX15 reported as uncertain significance for Cardioencephalomyopathy, fatal infantile, due to cytochrome c oxidase deficiency 2

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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: 7

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HGVS	dbSNP	gnomAD frequency
NM_004376.7(COX15):c.-84G>A	rs574143521	0.00036
NM_078470.6(COX15):c.929C>G (p.Pro310Arg)	rs138293000	0.00031
NM_078470.6(COX15):c.131G>A (p.Ser44Asn)	rs141506146	0.00011
NM_078470.6(COX15):c.532C>T (p.Arg178Cys)	rs192078749	0.00008
NM_078470.6(COX15):c.1015G>A (p.Val339Met)	rs141830307	0.00006
NM_078470.6(COX15):c.211C>T (p.Arg71Ter)	rs751819645	0.00001
NM_078470.6(COX15):c.679C>G (p.Leu227Val)	rs2133606863

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