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Items: 8

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
IRF2BPL
(P699H)
Single nucleotide variant
(missense variant)
Neurodevelopmental disorder with regression, abnormal movements, loss of speech, and seizures
GUncertain significance
IRF2BPL
(K641N)
Single nucleotide variant
(missense variant)
Neurodevelopmental disorder with regression, abnormal movements, loss of speech, and seizures
GUncertain significance
IRF2BPL
(A625V)
Single nucleotide variant
(missense variant)
Neurodevelopmental disorder with regression, abnormal movements, loss of speech, and seizures
GUncertain significance
IRF2BPL
(G428D)
Single nucleotide variant
(missense variant)
Neurodevelopmental disorder with regression, abnormal movements, loss of speech, and seizures
GUncertain significance
IRF2BPL
(G400S)
Single nucleotide variant
(missense variant)
Neurodevelopmental disorder with regression, abnormal movements, loss of speech, and seizures
GLikely pathogenic
IRF2BPL
(N255I)
Single nucleotide variant
(missense variant)
Neurodevelopmental disorder with regression, abnormal movements, loss of speech, and seizures
GUncertain significance
IRF2BPL
(S219Y)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
+1 more
GUncertain significance
IRF2BPL
(Q105*)
Single nucleotide variant
(nonsense)
Neurodevelopmental disorder with regression, abnormal movements, loss of speech, and seizures
GUncertain significance
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