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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
COX10, LOC105943586
(C243del)
Microsatellite
(inframe_deletion)
Mitochondrial complex 4 deficiency, nuclear type 3
+1 more
GUncertain significance
COX10, LOC105943586
(V255M)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
COX10, LOC105943586
(W286C)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
COX10, LOC105943586
Single nucleotide variant
(synonymous variant)
not provided
GLikely benign
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