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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
UBE4A
(R112H)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
+1 more
GUncertain significance
UBE4A
(N209S)
Single nucleotide variant
(missense variant)
UBE4A-related disorder
GUncertain significance
UBE4A
(Q238H)
Single nucleotide variant
(missense variant)
UBE4A-related disorder
GUncertain significance
UBE4A
(H408L +1 more)
Single nucleotide variant
(missense variant)
UBE4A-related disorder
GUncertain significance
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