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Items: 6

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
OAT
Single nucleotide variant
(synonymous variant)
not provided
+1 more
GConflicting classifications of pathogenicity
OAT
Single nucleotide variant
(synonymous variant)
Ornithine aminotransferase deficiency
+1 more
GConflicting classifications of pathogenicity
OAT
Single nucleotide variant
(intron variant)
not specified
+2 more
GBenign
OAT
(N118Y)
Single nucleotide variant
(missense variant +2 more)
not provided
GUncertain significance
OAT
Single nucleotide variant
(intron variant)
Ornithine aminotransferase deficiency
+1 more
GUncertain significance
OAT
Single nucleotide variant
(synonymous variant +1 more)
not provided
+2 more
GConflicting classifications of pathogenicity
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