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Items: 11

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
AKAP9
(R40K)
Single nucleotide variant
(missense variant)
Congenital long QT syndrome
+3 more
GConflicting classifications of pathogenicity
AKAP9
(C870Y)
Single nucleotide variant
(missense variant)
Long QT syndrome 11
+2 more
GConflicting classifications of pathogenicity
AKAP9
Single nucleotide variant
(synonymous variant)
Long QT syndrome
+1 more
GConflicting classifications of pathogenicity
AKAP9
(S1388L)
Single nucleotide variant
(missense variant)
Long QT syndrome 11
+3 more
GConflicting classifications of pathogenicity
AKAP9
(T105K +1 more)
Single nucleotide variant
(missense variant)
Long QT syndrome 11
GUncertain significance
AKAP9
(R2165Q +2 more)
Single nucleotide variant
(missense variant)
Cardiovascular phenotype
+2 more
GConflicting classifications of pathogenicity
AKAP9
(I1035V +2 more)
Single nucleotide variant
(missense variant)
Long QT syndrome 11
GUncertain significance
AKAP9
(K3230R +2 more)
Single nucleotide variant
(missense variant)
Long QT syndrome 11
+2 more
GConflicting classifications of pathogenicity
AKAP9
(T3399N +2 more)
Single nucleotide variant
(missense variant)
Long QT syndrome 11
+1 more
GUncertain significance
AKAP9
(R3756K +2 more)
Single nucleotide variant
(missense variant)
Long QT syndrome 11
+2 more
GUncertain significance
AKAP9
(R3779Q +2 more)
Single nucleotide variant
(missense variant)
Long QT syndrome 11
+2 more
GUncertain significance
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