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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
FASTKD2
(P151L)
Single nucleotide variant
(missense variant)
Mitochondrial complex IV deficiency, nuclear type 1
GUncertain significance
FASTKD2
(Q228H)
Single nucleotide variant
(missense variant)
Mitochondrial complex IV deficiency, nuclear type 1
+2 more
GConflicting classifications of pathogenicity
FASTKD2
(Q564*)
Single nucleotide variant
(nonsense)
Mitochondrial complex IV deficiency, nuclear type 1
GPathogenic
FASTKD2
(P599L)
Single nucleotide variant
(missense variant)
Combined oxidative phosphorylation deficiency 44
GUncertain significance
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