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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
PTCD3
(W65S)
Single nucleotide variant
(missense variant)
Combined oxidative phosphorylation deficiency 51
GUncertain significance
PTCD3
(R524L)
Single nucleotide variant
(missense variant)
Combined oxidative phosphorylation deficiency 51
GUncertain significance
PTCD3
Single nucleotide variant
(synonymous variant)
Combined oxidative phosphorylation deficiency 51
GUncertain significance
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