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Items: 9

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
CTNNA3
Deletion
(splice donor variant)
Arrhythmogenic right ventricular dysplasia 13
GUncertain significance
CTNNA3
(A660V)
Single nucleotide variant
(missense variant)
Arrhythmogenic right ventricular dysplasia 13
+1 more
GUncertain significance
CTNNA3
(R543Q)
Single nucleotide variant
(missense variant)
Arrhythmogenic right ventricular dysplasia 13
GUncertain significance
CTNNA3
(R484H)
Single nucleotide variant
(missense variant)
Arrhythmogenic right ventricular dysplasia 13
GUncertain significance
CTNNA3
(M435V)
Single nucleotide variant
(missense variant)
Arrhythmogenic right ventricular dysplasia 13
+1 more
GConflicting classifications of pathogenicity
CTNNA3
(I411V)
Single nucleotide variant
(missense variant)
Arrhythmogenic right ventricular dysplasia 13
+1 more
GConflicting classifications of pathogenicity
CTNNA3
(P266S +1 more)
Single nucleotide variant
(missense variant)
Arrhythmogenic right ventricular dysplasia 13
GUncertain significance
CTNNA3
(Q260R +1 more)
Single nucleotide variant
(missense variant)
Arrhythmogenic right ventricular dysplasia 13
+2 more
GConflicting classifications of pathogenicity
CTNNA3
(V144A +1 more)
Single nucleotide variant
(missense variant)
Arrhythmogenic right ventricular dysplasia 13
GUncertain significance
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