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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
COA8
(E29K)
Single nucleotide variant
(missense variant +1 more)
Mitochondrial complex 4 deficiency, nuclear type 17
+1 more
GConflicting classifications of pathogenicity
COA8
(K118* +1 more)
Single nucleotide variant
(nonsense +1 more)
Mitochondrial complex 4 deficiency, nuclear type 17
GLikely pathogenic