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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
FASTKD2
(D398V)
Single nucleotide variant
(missense variant)
Mitochondrial complex IV deficiency, nuclear type 1
+2 more
GConflicting classifications of pathogenicity
FASTKD2
(L513fs)
Deletion
(frameshift variant)
Combined oxidative phosphorylation deficiency 44
GLikely pathogenic