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Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
AKAP9
(A25T)
Single nucleotide variant
(missense variant)
Ventricular tachycardia
GUncertain significance
AKAP9
(D356V)
Single nucleotide variant
(missense variant)
Long QT syndrome
+2 more
GUncertain significance
AKAP9
(V367M)
Single nucleotide variant
(missense variant)
Long QT syndrome
+3 more
GLikely benign
AKAP9
(E497*)
Single nucleotide variant
(nonsense)
Long QT syndrome 11
GLikely pathogenic
AKAP9
(A1194T)
Single nucleotide variant
(missense variant)
not provided
+4 more
GConflicting classifications of pathogenicity
AKAP9
Single nucleotide variant
(intron variant)
Cardiovascular phenotype
+2 more
GUncertain significance
AKAP9
(R1609Q)
Indel
(missense variant)
Ventricular fibrillation
+4 more
GConflicting classifications of pathogenicity
AKAP9
(D1758H)
Single nucleotide variant
(missense variant)
Ventricular fibrillation
GUncertain significance
AKAP9
(V1790G)
Single nucleotide variant
(missense variant)
Congenital long QT syndrome
+5 more
GConflicting classifications of pathogenicity
AKAP9
(E2438D +2 more)
Single nucleotide variant
(missense variant)
Cardiovascular phenotype
+2 more
GConflicting classifications of pathogenicity
AKAP9
(T2782I +2 more)
Single nucleotide variant
(missense variant)
Long QT syndrome
+1 more
GConflicting classifications of pathogenicity
AKAP9
(I2886V +2 more)
Single nucleotide variant
(missense variant)
not specified
+2 more
GConflicting classifications of pathogenicity
AKAP9
(R3038C +2 more)
Single nucleotide variant
(missense variant)
not specified
+1 more
GUncertain significance
AKAP9
(S3114fs +2 more)
Duplication
(frameshift variant)
Long QT syndrome
GUncertain significance
AKAP9
(S3341L +2 more)
Single nucleotide variant
(missense variant)
Long QT syndrome
GUncertain significance
AKAP9
(R3388T +2 more)
Single nucleotide variant
(missense variant)
Long QT syndrome
GUncertain significance
AKAP9
(P3759L +2 more)
Single nucleotide variant
(missense variant)
Cardiac arrest
GUncertain significance
AKAP9
(S3793C +2 more)
Single nucleotide variant
(missense variant)
Cardiovascular phenotype
+2 more
GUncertain significance
AKAP9
(S3833* +2 more)
Single nucleotide variant
(nonsense)
Long QT syndrome
GUncertain significance
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