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Items: 14

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
SLC35C1
(R10K)
Single nucleotide variant
(5 prime UTR variant +1 more)
Leukocyte adhesion deficiency type II
+2 more
GUncertain significance
SLC35C1
(G30R +1 more)
Single nucleotide variant
(missense variant)
Leukocyte adhesion deficiency type II
+1 more
GUncertain significance
SLC35C1
(L39S +1 more)
Single nucleotide variant
(missense variant)
Leukocyte adhesion deficiency type II
+1 more
GUncertain significance
SLC35C1
(T51A +1 more)
Single nucleotide variant
(missense variant)
Leukocyte adhesion deficiency type II
+1 more
GUncertain significance
SLC35C1
(S54F +1 more)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
+1 more
GUncertain significance
SLC35C1
(V63I +1 more)
Single nucleotide variant
(missense variant)
Leukocyte adhesion deficiency type II
+1 more
GConflicting classifications of pathogenicity
SLC35C1
(L109V +1 more)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
SLC35C1
(V132M +1 more)
Single nucleotide variant
(missense variant)
Leukocyte adhesion deficiency type II
+1 more
GUncertain significance
SLC35C1
(N141T +1 more)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
SLC35C1
(V200I +1 more)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
+1 more
GConflicting classifications of pathogenicity
SLC35C1
(R256H +1 more)
Single nucleotide variant
(missense variant)
Leukocyte adhesion deficiency type II
+1 more
GConflicting classifications of pathogenicity
SLC35C1
(A259T +1 more)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
SLC35C1
(T258M +1 more)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
+1 more
GUncertain significance
SLC35C1
(E344G +1 more)
Single nucleotide variant
(missense variant)
Leukocyte adhesion deficiency type II
+1 more
GUncertain significance
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