ClinVar Miner

List of variants in gene COA8 reported as benign for Mitochondrial complex 4 deficiency, nuclear type 17

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
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Total variants: 2

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HGVS	dbSNP	gnomAD frequency
NM_001370595.2(COA8):c.476+19C>T	rs182242924	0.00201
NM_001370595.2(COA8):c.40C>G (p.Pro14Ala)	rs2274268

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