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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
ATL1
(R239C)
Single nucleotide variant
(missense variant)
Hereditary spastic paraplegia
+3 more
GPathogenic/Likely pathogenic
ATL1
(E308K)
Single nucleotide variant
(missense variant)
not provided
+2 more
GConflicting classifications of pathogenicity
ATL1
(F402L)
Single nucleotide variant
(missense variant)
Hereditary spastic paraplegia 3A
GUncertain significance
ATL1
(M408L)
Single nucleotide variant
(missense variant)
Hereditary spastic paraplegia 3A
GUncertain significance
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