ClinVar Miner

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

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Gene type:
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Total variants: 36
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HGVS dbSNP
NM_000018.3(ACADVL):c.1066A>G (p.Ile356Val) rs150140386
NM_000018.3(ACADVL):c.1077+15C>T rs202237278
NM_000018.3(ACADVL):c.1182+17C>A rs191276923
NM_000018.3(ACADVL):c.1182+3G>A rs376281637
NM_000018.3(ACADVL):c.1236G>A (p.Gln412=) rs745355288
NM_000018.3(ACADVL):c.1284G>A (p.Lys428=) rs35501596
NM_000018.3(ACADVL):c.1333-3T>C rs1057523216
NM_000018.3(ACADVL):c.138+10C>G rs1057523013
NM_000018.3(ACADVL):c.1434+14T>A rs202217537
NM_000018.3(ACADVL):c.1434+14T>C rs202217537
NM_000018.3(ACADVL):c.1532+20C>G rs1291717212
NM_000018.3(ACADVL):c.1532+7T>C rs534469222
NM_000018.3(ACADVL):c.1533-4T>A rs369986567
NM_000018.3(ACADVL):c.1569A>G (p.Gly523=) rs779048354
NM_000018.3(ACADVL):c.1581G>A (p.Pro527=) rs149436747
NM_000018.3(ACADVL):c.1605+6_1605+7delTGinsCA rs1064795676
NM_000018.3(ACADVL):c.1678+15C>T rs371402802
NM_000018.3(ACADVL):c.1679-19_1679-14delCACCCC rs754154374
NM_000018.3(ACADVL):c.1679-19_1679-14dupCACCCC rs754154374
NM_000018.3(ACADVL):c.1751+18G>A rs528002997
NM_000018.3(ACADVL):c.1824C>T (p.Ile608=) rs146115467
NM_000018.3(ACADVL):c.1827+8T>C rs941400018
NM_000018.3(ACADVL):c.1839G>A (p.Arg613=) rs79125791
NM_000018.3(ACADVL):c.1866G>A (p.Gln622=) rs373898227
NM_000018.3(ACADVL):c.277+6G>A rs776422793
NM_000018.3(ACADVL):c.369C>T (p.Asp123=) rs374524648
NM_000018.3(ACADVL):c.477+12C>G rs1057523521
NM_000018.3(ACADVL):c.477+17G>A rs375076326
NM_000018.3(ACADVL):c.622+12C>A rs374633807
NM_000018.3(ACADVL):c.663C>T (p.Ser221=) rs144255994
NM_000018.3(ACADVL):c.678C>A (p.Ala226=) rs372114185
NM_000018.3(ACADVL):c.68G>A (p.Arg23Gln) rs34153370
NM_000018.3(ACADVL):c.753-27C>T rs374911841
NM_000018.3(ACADVL):c.756T>C (p.Asn252=) rs143233413
NM_000018.3(ACADVL):c.759G>A (p.Gly253=) rs148073142
NM_000018.3(ACADVL):c.972T>C (p.Gly324=) rs1555528483

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