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Items: 5

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
PRKCG
Single nucleotide variant
(synonymous variant)
Spinocerebellar ataxia type 14
+2 more
GBenign
PRKCG
Single nucleotide variant
(synonymous variant)
Spinocerebellar ataxia type 14
+1 more
GBenign
PRKCG
Single nucleotide variant
(intron variant)
not provided
+1 more
GBenign
PRKCG
(R239W)
Single nucleotide variant
(missense variant)
Spinocerebellar ataxia type 14
GUncertain significance
PRKCG
(V583M)
Single nucleotide variant
(missense variant)
Spinocerebellar ataxia type 14
+1 more
GConflicting classifications of pathogenicity
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