ClinVar Miner

List of variants in gene ACAD9 reported as likely benign by GeneDx

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 38
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HGVS dbSNP gnomAD frequency
NM_014049.5(ACAD9):c.633+163T>A rs76764354 0.02560
NM_014049.4(ACAD9):c.-168T>C rs183973851 0.01194
NM_014049.5(ACAD9):c.150+87C>T rs111805092 0.00832
NM_014049.5(ACAD9):c.808+22G>A rs192075896 0.00681
NM_014049.5(ACAD9):c.1563+212G>A rs189588655 0.00525
NM_014049.5(ACAD9):c.1149+51C>T rs139008397 0.00522
NM_014049.5(ACAD9):c.1485+25C>A rs61300654 0.00477
NM_014049.5(ACAD9):c.1278+89G>A rs77143896 0.00339
NM_014049.5(ACAD9):c.633+76C>A rs115131918 0.00337
NM_014049.5(ACAD9):c.808+133A>G rs137992130 0.00315
NM_014049.5(ACAD9):c.1278+174C>T rs144152795 0.00149
NM_014049.5(ACAD9):c.151-250A>C rs150724622 0.00149
NM_014049.5(ACAD9):c.454-20T>C rs140366274 0.00088
NM_014049.5(ACAD9):c.1221A>G (p.Thr407=) rs139048558 0.00066
NM_014049.5(ACAD9):c.432G>A (p.Ala144=) rs140225132 0.00061
NM_014049.5(ACAD9):c.513C>T (p.Ser171=) rs111716284 0.00027
NM_014049.5(ACAD9):c.1233G>A (p.Pro411=) rs754767509 0.00013
NM_014049.5(ACAD9):c.150+8G>A rs528508645 0.00011
NM_014049.5(ACAD9):c.808+18G>A rs371813160 0.00008
NM_014049.5(ACAD9):c.808+20G>A rs531217490 0.00008
NM_014049.5(ACAD9):c.30C>T (p.Thr10=) rs371199008 0.00007
NM_014049.5(ACAD9):c.1278+9C>G rs372636698 0.00006
NM_014049.5(ACAD9):c.981C>T (p.Cys327=) rs537393165 0.00004
NM_014049.5(ACAD9):c.1223G>C (p.Arg408Thr) rs863223871 0.00003
NM_014049.5(ACAD9):c.662A>G (p.Asn221Ser) rs761452056 0.00003
NM_014049.5(ACAD9):c.675G>A (p.Val225=) rs150459138 0.00002
NM_014049.5(ACAD9):c.634-5C>T rs202115420 0.00001
NM_014049.5(ACAD9):c.-11C>T rs959271889
NM_014049.5(ACAD9):c.1059T>G (p.Ala353=) rs1553731808
NM_014049.5(ACAD9):c.1134G>A (p.Glu378=) rs1017503875
NM_014049.5(ACAD9):c.1150-85G>A rs186712694
NM_014049.5(ACAD9):c.11G>T (p.Cys4Phe) rs863223872
NM_014049.5(ACAD9):c.1331C>T (p.Ala444Val) rs549861940
NM_014049.5(ACAD9):c.244+52G>A rs140606723
NM_014049.5(ACAD9):c.347-7C>T rs973931566
NM_014049.5(ACAD9):c.454-5T>C rs750934273
NM_014049.5(ACAD9):c.555-169_555-167del rs201894239
NM_014049.5(ACAD9):c.809-10T>C rs1553731310

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