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Items: 5

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
CASD1, SGCE
(Q352K +4 more)
Single nucleotide variant
(missense variant +1 more)
Myoclonic dystonia 11
GUncertain significance
CASD1, SGCE
(L184P +4 more)
Single nucleotide variant
(missense variant)
not provided
+1 more
GPathogenic/Likely pathogenic
CASD1, SGCE
(R102* +4 more)
Single nucleotide variant
(nonsense)
not provided
+1 more
GPathogenic
CASD1, SGCE
(F87L +3 more)
Single nucleotide variant
(missense variant +1 more)
Myoclonic dystonia 11
GUncertain significance
SGCE
(T32A)
Single nucleotide variant
(missense variant +1 more)
Myoclonic dystonia 11
GUncertain significance
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