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Items: 5

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
LOC126863253, UBA1
(P19L)
Single nucleotide variant
(missense variant)
Infantile-onset X-linked spinal muscular atrophy
GUncertain significance
LOC126863253, UBA1
Single nucleotide variant
(synonymous variant)
Infantile-onset X-linked spinal muscular atrophy
GUncertain significance
UBA1
(P168S)
Single nucleotide variant
(missense variant)
Infantile-onset X-linked spinal muscular atrophy
GBenign/Likely benign
UBA1
(V373M)
Single nucleotide variant
(missense variant)
Infantile-onset X-linked spinal muscular atrophy
+2 more
GUncertain significance
UBA1
(T531M)
Single nucleotide variant
(missense variant)
Infantile-onset X-linked spinal muscular atrophy
GUncertain significance
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