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Items: 5

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
UFL1-AS1, FUT9
(N34K)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
UFL1-AS1, FUT9
(T95M)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
FUT9, UFL1-AS1
(S114N)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
FUT9, UFL1-AS1
(S146T)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
UFL1-AS1, FUT9
(R328Q)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
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