ClinVar Miner

List of variants in gene ACADS reported by PreventionGenetics, part of Exact Sciences

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Gene type:
ClinVar version:
Total variants: 32
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HGVS dbSNP gnomAD frequency
NM_000017.4(ACADS):c.990C>T (p.Arg330=) rs3915 0.59445
NM_000017.4(ACADS):c.321T>C (p.Arg107=) rs3914 0.51709
NM_000017.4(ACADS):c.*21G>C rs3916 0.21460
NM_000017.4(ACADS):c.360C>T (p.Asn120=) rs76543640 0.01346
NM_000017.4(ACADS):c.625-83G>A rs150191962 0.01034
NM_000017.4(ACADS):c.522C>T (p.Gly174=) rs143925225 0.00169
NM_000017.4(ACADS):c.654A>C (p.Pro218=) rs149430391 0.00075
NM_000017.4(ACADS):c.655A>T (p.Thr219Ser) rs144815059 0.00075
NM_000017.4(ACADS):c.669G>A (p.Thr223=) rs17848089 0.00056
NM_000017.4(ACADS):c.795+9G>A rs370703070 0.00031
NM_000017.4(ACADS):c.*4C>T rs774815274 0.00009
NM_000017.4(ACADS):c.136C>T (p.Arg46Trp) rs121908003 0.00008
NM_000017.4(ACADS):c.327C>T (p.Cys109=) rs144083614 0.00007
NM_000017.4(ACADS):c.1210G>A (p.Gly404Arg) rs545737847 0.00006
NM_000017.4(ACADS):c.147C>G (p.Ala49=) rs202193021 0.00004
NM_000017.4(ACADS):c.663G>T (p.Gly221=) rs751023929 0.00004
NM_000017.4(ACADS):c.1031A>G (p.Glu344Gly) rs387906950 0.00001
NM_000017.4(ACADS):c.1173C>T (p.Tyr391=) rs766657084 0.00001
NM_000017.4(ACADS):c.332C>T (p.Ser111Phe) rs747339462 0.00001
NM_000017.4(ACADS):c.336C>T (p.Thr112=) rs768784437 0.00001
NM_000017.4(ACADS):c.337G>A (p.Gly113Arg) rs781528570 0.00001
NM_000017.4(ACADS):c.360+21C>G rs372974263 0.00001
NM_000017.4(ACADS):c.596C>T (p.Ala199Val) rs766579880 0.00001
NM_000017.4(ACADS):c.906G>A (p.Ala302=) rs763162492 0.00001
NM_000017.4(ACADS):c.194_200del (p.Leu65fs)
NM_000017.4(ACADS):c.22C>A (p.Arg8=)
NM_000017.4(ACADS):c.249C>T (p.Asp83=)
NM_000017.4(ACADS):c.361-2A>T
NM_000017.4(ACADS):c.625-89G>A
NM_000017.4(ACADS):c.682_683del (p.Glu228fs) rs786204691
NM_000017.4(ACADS):c.826del (p.Ala276fs)
NM_000017.4(ACADS):c.988_990delinsTGT (p.Arg330Cys) rs796051906

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