ClinVar Miner

List of variants in gene ACADVL reported as benign

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Total variants: 33
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HGVS dbSNP
NM_000018.4(ACADVL):c.1038G>A (p.Ala346=) rs8064573
NM_000018.4(ACADVL):c.1066A>G (p.Ile356Val) rs150140386
NM_000018.4(ACADVL):c.1077+15C>T rs202237278
NM_000018.4(ACADVL):c.1182+17C>A rs191276923
NM_000018.4(ACADVL):c.1284G>A (p.Lys428=) rs35501596
NM_000018.4(ACADVL):c.128G>A (p.Gly43Asp) rs2230178
NM_000018.4(ACADVL):c.1473A>G (p.Leu491=) rs150518187
NM_000018.4(ACADVL):c.1533G>A (p.Arg511=) rs886038214
NM_000018.4(ACADVL):c.1581G>A (p.Pro527=) rs149436747
NM_000018.4(ACADVL):c.1600G>A (p.Glu534Lys) rs2230180
NM_000018.4(ACADVL):c.1605+6T>C rs17671352
NM_000018.4(ACADVL):c.1605+7G>A rs572010910
NM_000018.4(ACADVL):c.1678+23C>T rs147546456
NM_000018.4(ACADVL):c.1824C>T (p.Ile608=) rs146115467
NM_000018.4(ACADVL):c.1828-4C>G rs184559206
NM_000018.4(ACADVL):c.1839G>A (p.Arg613=) rs79125791
NM_000018.4(ACADVL):c.194C>T (p.Pro65Leu) rs28934585
NM_000018.4(ACADVL):c.1965C>T (p.Phe655=) rs9674
NM_000018.4(ACADVL):c.308A>G (p.Lys103Arg) rs140566084
NM_000018.4(ACADVL):c.343-14T>C
NM_000018.4(ACADVL):c.478-106del rs370388543
NM_000018.4(ACADVL):c.478-22_478-21del rs60400822
NM_000018.4(ACADVL):c.622+12C>A rs374633807
NM_000018.4(ACADVL):c.623-8C>T rs144996066
NM_000018.4(ACADVL):c.63-35G>A rs774905326
NM_000018.4(ACADVL):c.636C>T (p.Ala212=) rs76547988
NM_000018.4(ACADVL):c.663C>T (p.Ser221=) rs144255994
NM_000018.4(ACADVL):c.68G>A (p.Arg23Gln) rs34153370
NM_000018.4(ACADVL):c.693T>A (p.Ser231=) rs77763289
NM_000018.4(ACADVL):c.753-27C>T rs374911841
NM_000018.4(ACADVL):c.780G>A (p.Thr260=) rs140871321
NM_000018.4(ACADVL):c.879-50G>T
NM_000018.4(ACADVL):c.963C>T (p.Asn321=) rs568118142

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