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Items: 21

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
IDUA, SLC26A1
Single nucleotide variant
(synonymous variant +2 more)
not provided
+2 more
GBenign
IDUA, SLC26A1
Deletion
(non-coding transcript variant +1 more)
Mucopolysaccharidosis type 1
IDUA, SLC26A1
(L18P)
Single nucleotide variant
(missense variant +2 more)
Hurler syndrome
+2 more
GConflicting classifications of pathogenicity
IDUA, SLC26A1
Single nucleotide variant
(intron variant +2 more)
Mucopolysaccharidosis type 1
IDUA, SLC26A1
(H33Q)
Single nucleotide variant
(missense variant +2 more)
Mucopolysaccharidosis type 1
IDUA, SLC26A1
(G51D)
Single nucleotide variant
(missense variant +2 more)
Mucopolysaccharidosis type 1
IDUA, SLC26A1
Deletion
(3 prime UTR variant +2 more)
Mucopolysaccharidosis type 1
+1 more
GConflicting classifications of pathogenicity
IDUA, SLC26A1
(P55fs)
Deletion
(3 prime UTR variant +3 more)
not provided
GPathogenic
IDUA, SLC26A1
(Y64fs)
Deletion
(3 prime UTR variant +3 more)
Hurler syndrome
+2 more
GPathogenic/Likely pathogenic
IDUA, SLC26A1
(Q70*)
Single nucleotide variant
(3 prime UTR variant +3 more)
IDUA-related disorder
+7 more
GPathogenic
IDUA, SLC26A1
Single nucleotide variant
(3 prime UTR variant +3 more)
not specified
+2 more
GConflicting classifications of pathogenicity
IDUA, SLC26A1
(A79T)
Single nucleotide variant
(3 prime UTR variant +3 more)
not specified
+4 more
GBenign/Likely benign; other
IDUA, SLC26A1
(H82P)
Single nucleotide variant
(3 prime UTR variant +3 more)
not provided
+3 more
GConflicting classifications of pathogenicity
IDUA, SLC26A1
(H82Q)
Single nucleotide variant
(3 prime UTR variant +3 more)
not specified
+4 more
GConflicting classifications of pathogenicity; other
IDUA, SLC26A1
(T99I)
Single nucleotide variant
(3 prime UTR variant +3 more)
not specified
+2 more
GBenign
IDUA, SLC26A1
(R100K)
Single nucleotide variant
(3 prime UTR variant +3 more)
not provided
+1 more
GUncertain significance
IDUA, SLC26A1
Single nucleotide variant
(splice donor variant +2 more)
Hurler syndrome
+2 more
GPathogenic/Likely pathogenic
IDUA, SLC26A1
Single nucleotide variant
(3 prime UTR variant +1 more)
Hurler syndrome
+4 more
GBenign
IDUA, SLC26A1
Single nucleotide variant
(3 prime UTR variant +1 more)
not provided
+2 more
GConflicting classifications of pathogenicity
SLC26A1, IDUA
(R538W)
Single nucleotide variant
(missense variant +1 more)
not provided
GConflicting classifications of pathogenicity
IDUA, SLC26A1
(W249*)
Single nucleotide variant
(nonsense +1 more)
Hypersulfaturia
+2 more
GConflicting classifications of pathogenicity
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