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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
IRF2BPL
(Q497*)
Single nucleotide variant
(nonsense)
Neurodevelopmental disorder with regression, abnormal movements, loss of speech, and seizures
GLikely pathogenic
IRF2BPL
(K201*)
Single nucleotide variant
(nonsense)
Neurodevelopmental disorder with regression, abnormal movements, loss of speech, and seizures
GLikely pathogenic
IRF2BPL
(Q167*)
Single nucleotide variant
(nonsense)
Neurodevelopmental disorder with regression, abnormal movements, loss of speech, and seizures
+2 more
GPathogenic/Likely pathogenic
IRF2BPL
(Q103fs)
Insertion
(frameshift variant)
Neurodevelopmental disorder with regression, abnormal movements, loss of speech, and seizures
GLikely pathogenic
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