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Items: 5

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
NDUFS8
(R2C)
Single nucleotide variant
(missense variant)
Mitochondrial complex I deficiency, nuclear type 1
+4 more
GConflicting classifications of pathogenicity
NDUFS8
(P7T)
Single nucleotide variant
(missense variant)
Leigh syndrome
+2 more
GConflicting classifications of pathogenicity
NDUFS8
(R18L)
Single nucleotide variant
(missense variant)
Leigh syndrome
+1 more
GUncertain significance
NDUFS8
(P22S)
Single nucleotide variant
(missense variant)
Leigh syndrome
+2 more
GUncertain significance
NDUFS8
(K115E)
Single nucleotide variant
(missense variant)
Leigh syndrome
+1 more
GConflicting classifications of pathogenicity
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