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Items: 12

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
GLB1
(D343G +3 more)
Single nucleotide variant
(missense variant)
Infantile GM1 gangliosidosis
GUncertain significance
GLB1
(R442Q +3 more)
Single nucleotide variant
(missense variant)
Infantile GM1 gangliosidosis
+5 more
GPathogenic/Likely pathogenic
GLB1
(V330fs +3 more)
Deletion
(frameshift variant)
Mucopolysaccharidosis, MPS-IV-B
+3 more
GPathogenic
GLB1
(F357fs +3 more)
Indel
(frameshift variant)
Infantile GM1 gangliosidosis
GLikely pathogenic
GLB1
(G210V +3 more)
Single nucleotide variant
(missense variant)
GM1 gangliosidosis type 3
GUncertain significance
GLB1
(N247D +3 more)
Single nucleotide variant
(missense variant)
Infantile GM1 gangliosidosis
GUncertain significance
GLB1
(T208I +2 more)
Single nucleotide variant
(missense variant +1 more)
GM1 gangliosidosis type 2
GUncertain significance
GLB1
(L142fs +3 more)
Microsatellite
(frameshift variant)
Infantile GM1 gangliosidosis
GUncertain significance
GLB1
(R148C +2 more)
Single nucleotide variant
(missense variant +1 more)
Infantile GM1 gangliosidosis
+5 more
GPathogenic/Likely pathogenic
GLB1
(T82M +3 more)
Single nucleotide variant
(missense variant)
GM1 gangliosidosis type 3
+6 more
GPathogenic/Likely pathogenic
GLB1, LOC129936434
+1 more
Duplication
(5 prime UTR variant +1 more)
GM1 gangliosidosis
+4 more
GPathogenic
GLB1, LOC129936434
+1 more
Deletion
(5 prime UTR variant +1 more)
Infantile GM1 gangliosidosis
+5 more
GPathogenic/Likely pathogenic
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