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Items: 9

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
TRDN
(Q727*)
Single nucleotide variant
(nonsense)
Catecholaminergic polymorphic ventricular tachycardia 1
+3 more
GUncertain significance
TRDN
(P601A)
Single nucleotide variant
(missense variant)
Cardiovascular phenotype
+3 more
GUncertain significance
TRDN
(E571D)
Single nucleotide variant
(missense variant)
not provided
+3 more
GConflicting classifications of pathogenicity
TRDN
(I534R)
Single nucleotide variant
(missense variant)
not provided
+3 more
GUncertain significance
TRDN
(E398V +1 more)
Single nucleotide variant
(missense variant)
Cardiovascular phenotype
+4 more
GConflicting classifications of pathogenicity
TRDN
(K318del)
Microsatellite
(inframe_deletion)
not provided
+1 more
GUncertain significance
TRDN
(E168fs)
Deletion
(frameshift variant)
not provided
GLikely pathogenic
TRDN
(G22V)
Single nucleotide variant
(missense variant)
not provided
+1 more
GUncertain significance
TRDN
Deletion
(inframe_deletion)
not provided
+1 more
GUncertain significance
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