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Links from MedGen

Items: 12

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
ATXN10
Single nucleotide variant
(splice donor variant)
Spinocerebellar ataxia type 10
GUncertain significance
ATXN10
(Q325* +1 more)
Single nucleotide variant
(nonsense)
Spinocerebellar ataxia type 10
GUncertain significance
ATXN10
(G135V +1 more)
Single nucleotide variant
(missense variant)
Spinocerebellar ataxia type 10
GUncertain significance
ATXN10, LOC130067689
Single nucleotide variant
(intron variant)
Spinocerebellar ataxia type 10
GUncertain significance
ATXN10
(R5G)
Single nucleotide variant
(missense variant)
Spinocerebellar ataxia type 10
GUncertain significance
ATXN10
Single nucleotide variant
(synonymous variant)
not specified
+2 more
GLikely benign
LOC107181287, ATXN10
+1 more
Microsatellite
(intron variant)
Spinocerebellar ataxia type 10
Gnot provided
ATXN10, LOC107181287
+1 more
Microsatellite
(intron variant)
Spinocerebellar ataxia type 10
GPathogenic
ATXN10, LOC107181287
+1 more
Microsatellite
Spinocerebellar ataxia type 10
GPathogenic
ATXN10, LOC107181287
+1 more
Microsatellite
Spinocerebellar ataxia type 10
GPathogenic
ATXN10, LOC107181287
+1 more
Microsatellite
Spinocerebellar ataxia type 10
GPathogenic
ATXN10, LOC107181287
+1 more
Microsatellite
Spinocerebellar ataxia type 10
GBenign
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