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Items: 5

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
CCT5
Single nucleotide variant
(5 prime UTR variant +1 more)
not provided
+1 more
GBenign
CCT5
Single nucleotide variant
(5 prime UTR variant +1 more)
not provided
+1 more
GBenign
CCT5
Single nucleotide variant
(synonymous variant +1 more)
Hereditary sensory and autonomic neuropathy with spastic paraplegia
+1 more
GBenign
CCT5
Single nucleotide variant
(synonymous variant)
Hereditary sensory and autonomic neuropathy with spastic paraplegia
+1 more
GBenign
CCT5
Single nucleotide variant
(intron variant)
Hereditary sensory and autonomic neuropathy with spastic paraplegia
+1 more
GBenign
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