ClinVar Miner

List of variants in gene ACAD9 reported as benign by GeneDx

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 62
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HGVS dbSNP gnomAD frequency
NM_014049.5(ACAD9):c.347-20C>T rs1683791 0.58733
NM_014049.5(ACAD9):c.453+305_453+307dup rs35399456 0.58572
NM_014049.5(ACAD9):c.555-150C>T rs1683804 0.58174
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.882+198A>G rs1680794 0.43900
NM_014049.5(ACAD9):c.1278+226C>T rs1680788 0.43881
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.346+331C>A rs1680781 0.40178
NM_014049.5(ACAD9):c.555-116C>G rs789213 0.25543
NM_014049.5(ACAD9):c.245-285A>C rs1683811 0.25474
NM_014049.5(ACAD9):c.1476C>T (p.Pro492=) rs876755 0.24221
NM_014049.5(ACAD9):c.1359-193G>A rs876756 0.24099
NM_014049.5(ACAD9):c.1150-192T>C rs2630252 0.23200
NM_014049.5(ACAD9):c.882+196T>C rs1680795 0.21775
NM_014049.5(ACAD9):c.959-163G>A rs66521976 0.14366
NM_014049.5(ACAD9):c.959-300G>A rs66903181 0.14125
NM_014049.5(ACAD9):c.633+199G>A rs34638819 0.13015
NM_014049.5(ACAD9):c.1358+152T>C rs13081342 0.10526
NM_014049.5(ACAD9):c.1278+150C>T rs35020699 0.10117
NM_014049.5(ACAD9):c.245-169A>T rs6806468 0.09167
NM_014049.5(ACAD9):c.453+281C>T rs62268191 0.05246
NM_014049.5(ACAD9):c.347-309T>C rs144311840 0.05185
NM_014049.5(ACAD9):c.346+63A>G rs10460833 0.04867
NM_014049.5(ACAD9):c.151-200T>C rs75748817 0.04866
NM_014049.5(ACAD9):c.-44_-41dup rs387906242 0.04863
NM_014049.5(ACAD9):c.1359-196T>C rs6782832 0.04655
NM_014049.5(ACAD9):c.1278+107G>A rs7652449 0.04648
NM_014049.5(ACAD9):c.1485+57T>C rs16852179 0.04648
NM_014049.5(ACAD9):c.1150-154C>T rs7651896 0.04645
NM_014049.5(ACAD9):c.1278+153C>T rs7652295 0.04645
NM_014049.5(ACAD9):c.1358+198G>A rs62265266 0.04633
NM_014049.5(ACAD9):c.1358+204G>C rs62265267 0.04633
NM_014049.5(ACAD9):c.1358+137C>G rs115864277 0.04271
NM_014049.5(ACAD9):c.347-149G>A rs143463639 0.04229
NM_014049.5(ACAD9):c.1149+57C>T rs73210609 0.02968
NM_014049.5(ACAD9):c.976G>A (p.Ala326Thr) rs115532916 0.02662
NM_014049.5(ACAD9):c.1563+237G>C rs16852182 0.02627
NM_014049.5(ACAD9):c.787T>C (p.Leu263=) rs1979529 0.02566
NM_014049.5(ACAD9):c.882+214C>T rs115920138 0.01977
NM_014049.5(ACAD9):c.1359-302A>G rs116630465 0.01976
NM_014049.5(ACAD9):c.1430G>A (p.Arg477Gln) rs4494951 0.01364
NM_014049.5(ACAD9):c.454-19C>A rs145442792 0.00368
NM_014049.5(ACAD9):c.554+20G>A rs201186311 0.00329
NM_014049.5(ACAD9):c.988A>C (p.Lys330Gln) rs79530903 0.00107
NM_014049.5(ACAD9):c.-65GT[4] rs397874507
NM_014049.5(ACAD9):c.1563+129T>G rs72973231
NM_014049.5(ACAD9):c.1563+217_1563+218del rs143672172
NM_014049.5(ACAD9):c.245-311_245-309del rs145182927
NM_014049.5(ACAD9):c.346+160G>C rs1680780
NM_014049.5(ACAD9):c.347-68dup rs11379527
NM_014049.5(ACAD9):c.808+62G>T rs2340466
NM_014049.5(ACAD9):c.808+63GT[14] rs63473460
NM_014049.5(ACAD9):c.808+63GT[19] rs63473460
NM_014049.5(ACAD9):c.808+63GT[21] rs63473460
NM_014049.5(ACAD9):c.808+63GT[22] rs63473460
NM_014049.5(ACAD9):c.808+63GT[23] rs63473460
NM_014049.5(ACAD9):c.809-103TGGA[10] rs370353055
NM_014049.5(ACAD9):c.809-103TGGA[11] rs370353055
NM_014049.5(ACAD9):c.959-145G>T rs1683776

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