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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
NDUFS7
(V122M)
Single nucleotide variant
(missense variant)
Mitochondrial complex 1 deficiency, nuclear type 3
+2 more
GPathogenic/Likely pathogenic
NDUFS7
(Y179*)
Single nucleotide variant
(nonsense)
Mitochondrial complex 1 deficiency, nuclear type 3
GLikely pathogenic