ClinVar Miner

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

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Gene type:
ClinVar version:
Total variants: 46
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HGVS dbSNP gnomAD frequency
NM_000018.4(ACADVL):c.879-79T>C rs114612853 0.00484
NM_000018.4(ACADVL):c.478-196A>C rs149152410 0.00336
NM_000018.4(ACADVL):c.1839G>A (p.Arg613=) rs79125791 0.00254
NM_000018.4(ACADVL):c.1752-36G>A rs200709964 0.00173
NM_000018.4(ACADVL):c.1678+23C>T rs147546456 0.00163
NM_000018.4(ACADVL):c.663C>T (p.Ser221=) rs144255994 0.00116
NM_000018.4(ACADVL):c.780G>A (p.Thr260=) rs140871321 0.00108
NM_000018.4(ACADVL):c.1284G>A (p.Lys428=) rs35501596 0.00061
NM_000018.4(ACADVL):c.1824C>T (p.Ile608=) rs146115467 0.00058
NM_000018.4(ACADVL):c.1077+15C>T rs202237278 0.00041
NM_000018.4(ACADVL):c.1581G>A (p.Pro527=) rs149436747 0.00035
NM_000018.4(ACADVL):c.1678+15C>T rs371402802 0.00029
NM_000018.4(ACADVL):c.1533-4T>A rs369986567 0.00026
NM_000018.4(ACADVL):c.1751+18G>A rs528002997 0.00024
NM_000018.4(ACADVL):c.759G>A (p.Gly253=) rs148073142 0.00014
NM_000018.4(ACADVL):c.756T>C (p.Asn252=) rs143233413 0.00013
NM_000018.4(ACADVL):c.*8C>T rs370513576 0.00011
NM_000018.4(ACADVL):c.622+12C>A rs374633807 0.00011
NM_000018.4(ACADVL):c.1182+17C>A rs191276923 0.00008
NM_000018.4(ACADVL):c.1828-20C>T rs757145035 0.00003
NM_000018.4(ACADVL):c.369C>T (p.Asp123=) rs374524648 0.00003
NM_000018.4(ACADVL):c.1827+8T>C rs941400018 0.00002
NM_000018.4(ACADVL):c.1866G>A (p.Gln622=) rs373898227 0.00002
NM_000018.4(ACADVL):c.477+12C>G rs1057523521 0.00002
NM_000018.4(ACADVL):c.957G>A (p.Ser319=) rs143870522 0.00002
NM_000018.4(ACADVL):c.1569A>G (p.Gly523=) rs779048354 0.00001
NM_000018.4(ACADVL):c.864C>T (p.Phe288=) rs753748672 0.00001
NM_000018.4(ACADVL):c.1182+3G>A rs376281637
NM_000018.4(ACADVL):c.1236G>A (p.Gln412=) rs745355288
NM_000018.4(ACADVL):c.1333-3T>C rs1057523216
NM_000018.4(ACADVL):c.1434+14T>A rs202217537
NM_000018.4(ACADVL):c.1434+14T>C rs202217537
NM_000018.4(ACADVL):c.1532+20C>G rs1291717212
NM_000018.4(ACADVL):c.1532+7T>C rs534469222
NM_000018.4(ACADVL):c.1605+6_1605+7inv
NM_000018.4(ACADVL):c.1679-35CCCCCA[2] rs754154374
NM_000018.4(ACADVL):c.1679-35CCCCCA[4] rs754154374
NM_000018.4(ACADVL):c.277+6G>A rs776422793
NM_000018.4(ACADVL):c.278-31_278-18del rs2071164779
NM_000018.4(ACADVL):c.477+17G>A rs375076326
NM_000018.4(ACADVL):c.477+50A>T rs150033153
NM_000018.4(ACADVL):c.678C>A (p.Ala226=) rs372114185
NM_000018.4(ACADVL):c.753-27C>T rs374911841
NM_000018.4(ACADVL):c.855G>A (p.Glu285=) rs201509063
NM_000018.4(ACADVL):c.879-159C>G rs74562836
NM_000018.4(ACADVL):c.972T>C (p.Gly324=) rs1555528483

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