ClinVar Miner

List of variants in gene COA6 reported as benign for Cardioencephalomyopathy, fatal infantile, due to cytochrome c oxidase deficiency 4

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Gene type: Distinguish antisense genes from sense genes
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Total variants: 2

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HGVS	dbSNP	gnomAD frequency
NM_001206641.3(COA6):c.47G>C (p.Ser16Thr)	rs10910420	0.60769
NM_001206641.3(COA6):c.373-8dup	rs58896934

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