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Items: 5

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
CCT5
(M29T)
Single nucleotide variant
(missense variant +1 more)
Hereditary sensory and autonomic neuropathy with spastic paraplegia
+1 more
GUncertain significance
CCT5
Single nucleotide variant
(synonymous variant)
not provided
GLikely benign
CCT5
Single nucleotide variant
(synonymous variant)
not provided
+1 more
GLikely benign
CCT5
Single nucleotide variant
(synonymous variant)
Hereditary sensory and autonomic neuropathy with spastic paraplegia
+1 more
GConflicting classifications of pathogenicity
CCT5
(I362M +4 more)
Single nucleotide variant
(missense variant)
Hereditary sensory and autonomic neuropathy with spastic paraplegia
+1 more
GBenign
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