"Baylor Genetics"[submitter] AND "AKAP9"[gene] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 940058	NM_005751.5(AKAP9):c.48+5G>A	AKAP9, LOC129998788	Single nucleotide variant (intron variant)	not specified +3 more	GUncertain significance
Select item 519331	NM_005751.5(AKAP9):c.1204G>A (p.Glu402Lys)	AKAP9 (E402K)	Single nucleotide variant (missense variant)	Long QT syndrome 11 +2 more	GConflicting classifications of pathogenicity
Select item 2441804	NM_005751.5(AKAP9):c.1243G>A (p.Glu415Lys)	AKAP9 (E415K)	Single nucleotide variant (missense variant)	Long QT syndrome 11 +1 more	GUncertain significance
Select item 838911	NM_005751.5(AKAP9):c.4136C>T (p.Thr1379Met)	AKAP9 (T1379M)	Single nucleotide variant (missense variant)	Long QT syndrome 11 +2 more	GUncertain significance
Select item 191519	NM_005751.5(AKAP9):c.6176A>G (p.Glu2059Gly)	AKAP9 (E2059G +1 more)	Single nucleotide variant (missense variant)	Cardiovascular phenotype +5 more	GConflicting classifications of pathogenicity
Select item 191523	NM_005751.5(AKAP9):c.9763A>G (p.Arg3255Gly)	AKAP9 (R3255G +2 more)	Single nucleotide variant (missense variant)	Long QT syndrome 11 +5 more	GConflicting classifications of pathogenicity
Select item 1031572	NM_005751.5(AKAP9):c.9838C>G (p.Gln3280Glu)	AKAP9 (Q1495E +2 more)	Single nucleotide variant (missense variant)	Long QT syndrome 11	GUncertain significance

ClinVar