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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
AP4B1, AP4B1-AS1
(K543Q +2 more)
Single nucleotide variant
(missense variant)
Hereditary spastic paraplegia 47
GUncertain significance
AP4B1, AP4B1-AS1
(G568D +2 more)
Single nucleotide variant
(missense variant)
Hereditary spastic paraplegia 47
+1 more
GUncertain significance
AP4B1, AP4B1-AS1
(N245H +2 more)
Single nucleotide variant
(non-coding transcript variant +1 more)
Hereditary spastic paraplegia 47
+1 more
GUncertain significance
AP4B1, AP4B1-AS1
(L222fs +2 more)
Deletion
(non-coding transcript variant +1 more)
not provided
+1 more
GPathogenic
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