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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
COX10, LOC105943586
(P246S)
Single nucleotide variant
(missense variant)
Mitochondrial complex IV deficiency, nuclear type 1
+2 more
GUncertain significance
COX10, LOC105943586
(A261S)
Single nucleotide variant
(missense variant)
not provided
+2 more
GUncertain significance