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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
HECTD4
(D2296G +2 more)
Single nucleotide variant
(missense variant)
Neurodevelopmental disorder with seizures, spasticity, and complete or partial agenesis of the corpus callosum
GUncertain significance
HECTD4
(I1692T +1 more)
Single nucleotide variant
(missense variant)
Neurodevelopmental disorder with seizures, spasticity, and complete or partial agenesis of the corpus callosum
GUncertain significance
HECTD4
(T1638fs +1 more)
Deletion
(frameshift variant)
Neurodevelopmental disorder with seizures, spasticity, and complete or partial agenesis of the corpus callosum
GPathogenic
HECTD4
(L1038P)
Single nucleotide variant
(missense variant)
Neurodevelopmental disorder with seizures, spasticity, and complete or partial agenesis of the corpus callosum
GUncertain significance
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