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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
TRIT1
(A329V +2 more)
Single nucleotide variant
(missense variant +1 more)
Combined oxidative phosphorylation deficiency 35
GUncertain significance
TRIT1
(R327* +1 more)
Single nucleotide variant
(nonsense +2 more)
not provided
+3 more
GPathogenic/Likely pathogenic
TRIT1
(D97N)
Single nucleotide variant
(missense variant +2 more)
Combined oxidative phosphorylation deficiency 35
+1 more
GConflicting classifications of pathogenicity
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