ClinVar Miner

List of variants in gene ACAD9 reported as uncertain significance for acyl-CoA dehydrogenase 9 deficiency

Included ClinVar conditions (1):
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Gene type:
ClinVar version:
Total variants: 23
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HGVS dbSNP
NM_014049.4(ACAD9):c.-168T>C rs183973851
NM_014049.4(ACAD9):c.-91G>T rs749695064
NM_014049.4(ACAD9):c.976G>A rs115532916
NM_014049.5(ACAD9):c.-65_-64GT[6] rs397874507
NM_014049.5(ACAD9):c.1062C>T (p.Tyr354=) rs886057957
NM_014049.5(ACAD9):c.1069G>A (p.Glu357Lys) rs765411526
NM_014049.5(ACAD9):c.1190C>T (p.Ala397Val) rs768894091
NM_014049.5(ACAD9):c.1258C>T (p.Arg420Cys) rs202147766
NM_014049.5(ACAD9):c.1331C>T (p.Ala444Val) rs549861940
NM_014049.5(ACAD9):c.1398C>T (p.Thr466=) rs772732061
NM_014049.5(ACAD9):c.1405C>T (p.Arg469Trp) rs139145143
NM_014049.5(ACAD9):c.1415G>A (p.Arg472Gln) rs762081272
NM_014049.5(ACAD9):c.1474C>T (p.Pro492Ser) rs886057958
NM_014049.5(ACAD9):c.1496A>G (p.Asn499Ser) rs369787602
NM_014049.5(ACAD9):c.152A>T (p.Lys51Ile) rs149931573
NM_014049.5(ACAD9):c.195T>C (p.Asn65=) rs144978857
NM_014049.5(ACAD9):c.346+15del rs886057956
NM_014049.5(ACAD9):c.41C>T (p.Ala14Val) rs886057954
NM_014049.5(ACAD9):c.442A>G (p.Ile148Val) rs202119704
NM_014049.5(ACAD9):c.44G>C (p.Arg15Pro) rs886057955
NM_014049.5(ACAD9):c.453+2T>A rs1179305061
NM_014049.5(ACAD9):c.555T>G (p.Ser185Arg) rs781738719
NM_014049.5(ACAD9):c.928G>A (p.Val310Ile) rs139073821

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