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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
SPG11
(L2032fs +2 more)
Duplication
(frameshift variant)
Hereditary spastic paraplegia 11
GUncertain significance
SPG11
(S1521P)
Single nucleotide variant
(missense variant)
Hereditary spastic paraplegia 11
+1 more
GUncertain significance
SPG11
(L887F)
Single nucleotide variant
(missense variant)
Hereditary spastic paraplegia 11
GUncertain significance
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