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Items: 5

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
CNOT3
(S245fs)
Indel
(frameshift variant)
Intellectual developmental disorder with speech delay, autism, and dysmorphic facies
+1 more
GConflicting classifications of pathogenicity
CNOT3
(G493fs)
Deletion
(frameshift variant)
not provided
GPathogenic
CNOT3
(W622*)
Single nucleotide variant
(nonsense)
Intellectual developmental disorder with speech delay, autism, and dysmorphic facies
GPathogenic
CNOT3
(C643fs)
Deletion
(frameshift variant)
Intellectual developmental disorder with speech delay, autism, and dysmorphic facies
GPathogenic
CNOT3
(Q694*)
Single nucleotide variant
(nonsense)
Intellectual developmental disorder with speech delay, autism, and dysmorphic facies
GPathogenic
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