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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
COX10
(S103A)
Single nucleotide variant
(missense variant)
Mitochondrial complex 4 deficiency, nuclear type 3
+1 more
GUncertain significance
COX10, LOC105943586
(A261S)
Single nucleotide variant
(missense variant)
not provided
+2 more
GUncertain significance
COX10
Single nucleotide variant
(intron variant)
not specified
+3 more
GConflicting classifications of pathogenicity
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