ClinVar Miner

List of variants in gene ACADVL reported as uncertain significance by ARUP Laboratories, Molecular Genetics and Genomics,ARUP Laboratories

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Total variants: 26
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HGVS dbSNP
NM_000018.4(ACADVL):c.1006A>G (p.Ile336Val) rs146369181
NM_000018.4(ACADVL):c.1052C>A (p.Thr351Asn) rs796051911
NM_000018.4(ACADVL):c.1052C>T (p.Thr351Ile) rs796051911
NM_000018.4(ACADVL):c.1127T>C (p.Phe376Ser) rs758928307
NM_000018.4(ACADVL):c.1226C>T (p.Thr409Met) rs113994169
NM_000018.4(ACADVL):c.1281G>C (p.Trp427Cys) rs1567567312
NM_000018.4(ACADVL):c.1287G>A (p.Val429=) rs999226548
NM_000018.4(ACADVL):c.1552G>A (p.Gly518Ser) rs374507980
NM_000018.4(ACADVL):c.1567G>A (p.Gly523Arg) rs139425622
NM_000018.4(ACADVL):c.1591C>T (p.Arg531Trp) rs146379816
NM_000018.4(ACADVL):c.1616C>A (p.Ala539Asp) rs781613690
NM_000018.4(ACADVL):c.1733T>C (p.Met578Thr) rs375806217
NM_000018.4(ACADVL):c.1844G>A (p.Arg615Gln) rs148584617
NM_000018.4(ACADVL):c.1878G>A (p.Trp626Ter) rs1555529186
NM_000018.4(ACADVL):c.428G>A (p.Gly143Asp) rs1458941582
NM_000018.4(ACADVL):c.485G>A (p.Arg162His) rs754756970
NM_000018.4(ACADVL):c.495G>T (p.Glu165Asp) rs370169077
NM_000018.4(ACADVL):c.521T>C (p.Val174Ala) rs372684079
NM_000018.4(ACADVL):c.605T>C (p.Leu202Pro) rs398123090
NM_000018.4(ACADVL):c.747G>C (p.Trp249Cys) rs141167669
NM_000018.4(ACADVL):c.753-11T>G rs1555528341
NM_000018.4(ACADVL):c.756T>A (p.Asn252Lys) rs143233413
NM_000018.4(ACADVL):c.907A>G (p.Lys303Glu) rs369149696
NM_000018.4(ACADVL):c.947G>A (p.Arg316Gln) rs147366714
NM_000018.4(ACADVL):c.949G>A (p.Val317Met) rs1567565417
NM_000018.4(ACADVL):c.950T>C (p.Val317Ala) rs398123095

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