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Links from Gene

Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
LOC129993038, TRPC3
Single nucleotide variant
(5 prime UTR variant)
TRPC3-related condition
GLikely benign
TRPC3
(S213W +1 more)
Single nucleotide variant
(missense variant)
Spinocerebellar ataxia type 41
GUncertain significance
LOC129993038, TRPC3
(K4M)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
TRPC3
(E244K +1 more)
Single nucleotide variant
(missense variant)
Spinocerebellar ataxia type 41
GUncertain significance
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