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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
CCT5
(I395V +4 more)
Single nucleotide variant
(missense variant)
Hereditary sensory and autonomic neuropathy with spastic paraplegia
GUncertain significance
CCT5
(A337G +4 more)
Single nucleotide variant
(missense variant)
Hereditary sensory and autonomic neuropathy with spastic paraplegia
GUncertain significance
CCT5
Single nucleotide variant
(stop lost)
Hereditary sensory and autonomic neuropathy with spastic paraplegia
GUncertain significance
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