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Items: 5

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
NAA15
(T48N)
Single nucleotide variant
(missense variant)
Intellectual disability, autosomal dominant 50
GUncertain significance
NAA15
(W109*)
Single nucleotide variant
(nonsense)
Intellectual disability, autosomal dominant 50
GLikely pathogenic
NAA15
Deletion
(frameshift variant +1 more)
Intellectual disability, autosomal dominant 50
GLikely pathogenic
NAA15
(L373*)
Single nucleotide variant
(nonsense)
Intellectual disability, autosomal dominant 50
GLikely pathogenic
NAA15
(T574fs)
Duplication
(frameshift variant)
Intellectual disability, autosomal dominant 50
GPathogenic
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