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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
SACS
(R4325* +1 more)
Single nucleotide variant
(nonsense)
Spastic paraplegia
+1 more
GPathogenic/Likely pathogenic
SACS
(D2419G +1 more)
Single nucleotide variant
(missense variant)
Charlevoix-Saguenay spastic ataxia
GUncertain significance
SACS
(L1727S +1 more)
Single nucleotide variant
(missense variant)
Charlevoix-Saguenay spastic ataxia
GUncertain significance
SACS
(S1718fs +1 more)
Duplication
(frameshift variant)
not provided
+4 more
GPathogenic
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