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Items: 11

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
ZNF142
(R1210W +2 more)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
+1 more
GUncertain significance
ZNF142
(R1181Q +2 more)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
+1 more
GUncertain significance
ZNF142
(S1133T +2 more)
Single nucleotide variant
(missense variant)
Neurodevelopmental disorder with impaired speech and hyperkinetic movements
GUncertain significance
ZNF142
(R1081H +2 more)
Single nucleotide variant
(missense variant)
Neurodevelopmental disorder with impaired speech and hyperkinetic movements
GUncertain significance
ZNF142
(H1153Q +2 more)
Single nucleotide variant
(missense variant)
Neurodevelopmental disorder with impaired speech and hyperkinetic movements
GUncertain significance
ZNF142
(G1052fs +2 more)
Deletion
(frameshift variant)
Neurodevelopmental disorder with impaired speech and hyperkinetic movements
GLikely pathogenic
ZNF142
(R847W +2 more)
Single nucleotide variant
(missense variant)
not provided
+2 more
GUncertain significance
ZNF142
(Q225P +2 more)
Single nucleotide variant
(missense variant)
Neurodevelopmental disorder with impaired speech and hyperkinetic movements
GUncertain significance
ZNF142
(R96C +2 more)
Single nucleotide variant
(missense variant)
Neurodevelopmental disorder with impaired speech and hyperkinetic movements
GUncertain significance
ZNF142
(M78V +2 more)
Single nucleotide variant
(missense variant)
Neurodevelopmental disorder with impaired speech and hyperkinetic movements
GUncertain significance
ZNF142
(Q9*)
Single nucleotide variant
(nonsense +1 more)
Inborn genetic diseases
+1 more
GUncertain significance
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