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Links from Gene

Items: 7

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
HECTD4
(L918R)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
HECTD4
(A1518T +1 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
HECTD4
(A3917V +1 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
(L1038P)
Single nucleotide variant
(missense variant)
Neurodevelopmental disorder with seizures, spasticity, and complete or partial agenesis of the corpus callosum
GUncertain significance
HECTD4
(D2296G +1 more)
Single nucleotide variant
(missense variant)
Neurodevelopmental disorder with seizures, spasticity, and complete or partial agenesis of the corpus callosum
GUncertain significance
HECTD4
(A3242fs +1 more)
Duplication
(frameshift variant)
Autism spectrum disorder
GLikely pathogenic
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