"Genome-Nilou Lab"[submitter] AND "ACAD9"[gene] - ClinVar - NCBI

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Items: 14

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 343189	NM_014049.5(ACAD9):c.-65GT[4]	ACAD9	Microsatellite (5 prime UTR variant +1 more)	Acyl-CoA dehydrogenase 9 deficiency +1 more	GBenign
Select item 1018	NM_014049.5(ACAD9):c.-44_-41dup	ACAD9	Duplication (5 prime UTR variant +1 more)	not provided +2 more	GConflicting classifications of pathogenicity
Select item 677920	NM_014049.5(ACAD9):c.346+160G>C	ACAD9	Single nucleotide variant (intron variant)	Acyl-CoA dehydrogenase 9 deficiency +1 more	GBenign
Select item 166634	NM_014049.5(ACAD9):c.347-20C>T	ACAD9	Single nucleotide variant (intron variant)	not specified +2 more	GBenign
Select item 166635	NM_014049.5(ACAD9):c.379A>C (p.Arg127=)	ACAD9	Single nucleotide variant (synonymous variant +1 more)	Acyl-CoA dehydrogenase 9 deficiency +2 more	GBenign
Select item 1185200	NM_014049.5(ACAD9):c.555-116C>G	ACAD9	Single nucleotide variant (intron variant)	not provided +1 more	GBenign
Select item 136253	NM_014049.5(ACAD9):c.976G>A (p.Ala326Thr)	ACAD9 (A326T)	Single nucleotide variant (missense variant +1 more)	not specified +2 more	GConflicting classifications of pathogenicity
Select item 1185201	NM_014049.5(ACAD9):c.1150-84T>G	ACAD9	Single nucleotide variant (intron variant)	not provided +1 more	GBenign
Select item 1188990	NM_014049.5(ACAD9):c.1279-76T>C	ACAD9	Single nucleotide variant (intron variant)	not provided +1 more	GBenign
Select item 166636	NM_014049.5(ACAD9):c.1279-7A>G	ACAD9	Single nucleotide variant (intron variant)	Acyl-CoA dehydrogenase 9 deficiency +2 more	GBenign
Select item 680076	NM_014049.5(ACAD9):c.1358+152T>C	ACAD9	Single nucleotide variant (intron variant)	Acyl-CoA dehydrogenase 9 deficiency +1 more	GBenign
Select item 1188991	NM_014049.5(ACAD9):c.1359-63T>C	ACAD9	Single nucleotide variant (intron variant)	not provided +1 more	GBenign
Select item 1195909	NM_014049.5(ACAD9):c.1366A>G (p.Lys456Glu)	ACAD9 (K456E)	Single nucleotide variant (missense variant +1 more)	Acyl-CoA dehydrogenase 9 deficiency	GUncertain significance
Select item 343203	NM_014049.5(ACAD9):c.1476C>T (p.Pro492=)	ACAD9	Single nucleotide variant (synonymous variant +1 more)	Acyl-CoA dehydrogenase 9 deficiency +1 more	GBenign