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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
COQ4
(R102C)
Single nucleotide variant
(synonymous variant +1 more)
Neonatal encephalomyopathy-cardiomyopathy-respiratory distress syndrome
GUncertain significance
COQ4
(F146C)
Single nucleotide variant
(missense variant +1 more)
Neonatal encephalomyopathy-cardiomyopathy-respiratory distress syndrome
+2 more
GConflicting classifications of pathogenicity
COQ4
(A153V)
Single nucleotide variant
(missense variant +1 more)
Inborn genetic diseases
+3 more
GConflicting classifications of pathogenicity
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