ClinVar Miner

List of variants reported as benign for acyl-CoA dehydrogenase 9 deficiency

Included ClinVar conditions (1):
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Total variants: 26
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HGVS dbSNP gnomAD frequency
NM_014049.5(ACAD9):c.347-20C>T rs1683791 0.58733
NM_014049.5(ACAD9):c.379A>C (p.Arg127=) rs1680778 0.45398
NM_014049.5(ACAD9):c.1150-84T>G rs1683777 0.43929
NM_014049.5(ACAD9):c.1279-7A>G rs1683787 0.43618
NM_014049.5(ACAD9):c.1279-76T>C rs1683786 0.43547
NM_014049.5(ACAD9):c.1359-63T>C rs876754 0.43543
NM_014049.5(ACAD9):c.555-116C>G rs789213 0.25543
NM_014049.5(ACAD9):c.1476C>T (p.Pro492=) rs876755 0.24221
NM_014049.5(ACAD9):c.1358+152T>C rs13081342 0.10526
NM_001394090.1(CFAP92):c.3281-2305C>T rs9830739 0.09177
NM_014049.5(ACAD9):c.-44_-41dup rs387906242 0.04863
NM_014049.5(ACAD9):c.976G>A (p.Ala326Thr) rs115532916 0.02662
NM_014049.5(ACAD9):c.787T>C (p.Leu263=) rs1979529 0.02566
NM_001394090.1(CFAP92):c.3281-2342G>A rs116106966 0.01973
NM_014049.5(ACAD9):c.1430G>A (p.Arg477Gln) rs4494951 0.01364
NM_001394090.1(CFAP92):c.3280+2181A>C rs114763241 0.01039
NM_014049.5(ACAD9):c.1683C>T (p.His561=) rs141647117 0.00531
NM_014049.5(ACAD9):c.988A>C (p.Lys330Gln) rs79530903 0.00107
NM_001394090.1(CFAP92):c.3281-2300G>A rs373417322 0.00009
NM_014049.5(ACAD9):c.102G>T (p.Pro34=) rs750501970 0.00001
NM_014049.5(ACAD9):c.-65GT[4] rs397874507
NM_014049.5(ACAD9):c.1331C>T (p.Ala444Val) rs549861940
NM_014049.5(ACAD9):c.1675C>A (p.Arg559Ser) rs138871762
NM_014049.5(ACAD9):c.346+160G>C rs1680780
NM_014049.5(ACAD9):c.808+63GT[14] rs63473460
NM_014049.5(ACAD9):c.976G>C (p.Ala326Pro) rs115532916

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