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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
COA6
(W59C +2 more)
Single nucleotide variant
(missense variant)
Cardioencephalomyopathy, fatal infantile, due to cytochrome c oxidase deficiency 4
GPathogenic
COA6
(W66R +2 more)
Single nucleotide variant
(missense variant)
Cardioencephalomyopathy, fatal infantile, due to cytochrome c oxidase deficiency 4
GPathogenic
COA6
(E87* +2 more)
Single nucleotide variant
(nonsense)
not provided
GUncertain significance
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