List of variants in gene ACAD9 reported as likely benign for acyl-CoA dehydrogenase 9 deficiency

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 23

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HGVS	dbSNP	gnomAD frequency
NM_014049.5(ACAD9):c.-44_-41dup	rs387906242	0.04863
NM_014049.5(ACAD9):c.988A>C (p.Lys330Gln)	rs79530903	0.00107
NM_014049.5(ACAD9):c.453+8A>G	rs199919500	0.00092
NM_014049.5(ACAD9):c.1022T>C (p.Leu341Ser)	rs141874052	0.00061
NM_014049.5(ACAD9):c.432G>A (p.Ala144=)	rs140225132	0.00061
NM_014049.5(ACAD9):c.195T>C (p.Asn65=)	rs144978857	0.00048
NM_014049.5(ACAD9):c.510G>A (p.Ala170=)	rs187374592	0.00042
NM_014049.5(ACAD9):c.152A>T (p.Lys51Ile)	rs149931573	0.00041
NM_014049.5(ACAD9):c.1020A>G (p.Gly340=)	rs138401844	0.00016
NM_014049.5(ACAD9):c.1233G>A (p.Pro411=)	rs754767509	0.00013
NM_014049.5(ACAD9):c.959-6C>T	rs368541873	0.00004
NM_014049.5(ACAD9):c.1533C>T (p.Thr511=)	rs376637096	0.00003
NM_014049.5(ACAD9):c.1551C>T (p.Leu517=)	rs751618594	0.00003
NM_014049.5(ACAD9):c.75G>T (p.Ala25=)	rs564435799	0.00003
NM_014049.5(ACAD9):c.254G>A (p.Arg85Gln)	rs573257268	0.00002
NM_014049.5(ACAD9):c.694G>A (p.Val232Ile)	rs371417658	0.00002
NM_014049.5(ACAD9):c.1062C>T (p.Tyr354=)	rs886057957	0.00001
NM_014049.5(ACAD9):c.1332C>T (p.Ala444=)	rs368597127	0.00001
NM_014049.5(ACAD9):c.1398C>T (p.Thr466=)	rs772732061	0.00001
NM_014049.5(ACAD9):c.1399G>A (p.Val467Ile)	rs369361055	0.00001
NM_014049.5(ACAD9):c.284A>C (p.Asp95Ala)	rs761565265	0.00001
NM_014049.5(ACAD9):c.1164G>A (p.Glu388=)	rs372572429
NM_014049.5(ACAD9):c.1331C>T (p.Ala444Val)	rs549861940

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