ClinVar Miner

List of variants in gene ACADVL reported as uncertain significance by Counsyl

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Total variants: 53
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HGVS dbSNP
NM_000018.4(ACADVL):c.1001T>G (p.Met334Arg) rs398123079
NM_000018.4(ACADVL):c.1009_1011del (p.Leu337del) rs1315330884
NM_000018.4(ACADVL):c.1019G>T (p.Gly340Val) rs934797393
NM_000018.4(ACADVL):c.1062_1064CAT[1] (p.Ile356del) rs754325237
NM_000018.4(ACADVL):c.1066A>G (p.Ile356Val) rs150140386
NM_000018.4(ACADVL):c.1077G>A (p.Ala359=) rs779458466
NM_000018.4(ACADVL):c.1096C>T (p.Arg366Cys) rs771874163
NM_000018.4(ACADVL):c.1103A>C (p.Gln368Pro) rs776063244
NM_000018.4(ACADVL):c.1153C>T (p.Arg385Trp) rs745832866
NM_000018.4(ACADVL):c.1183-15A>G rs765390290
NM_000018.4(ACADVL):c.1183-2dup rs1555528721
NM_000018.4(ACADVL):c.1198G>A (p.Val400Met) rs149116708
NM_000018.4(ACADVL):c.1246G>T (p.Ala416Ser) rs118204018
NM_000018.4(ACADVL):c.1273G>A (p.Ala425Thr) rs138834083
NM_000018.4(ACADVL):c.1328T>G (p.Met443Arg) rs886043236
NM_000018.4(ACADVL):c.1360G>A (p.Asp454Asn) rs1419606204
NM_000018.4(ACADVL):c.138+2dup rs1555527548
NM_000018.4(ACADVL):c.139-3C>T rs1555527630
NM_000018.4(ACADVL):c.1430G>A (p.Cys477Tyr) rs1555528803
NM_000018.4(ACADVL):c.1532G>C (p.Arg511Pro) rs200771970
NM_000018.4(ACADVL):c.1533-4T>A rs369986567
NM_000018.4(ACADVL):c.1591C>T (p.Arg531Trp) rs146379816
NM_000018.4(ACADVL):c.1617T>C (p.Ala539=) rs1555528948
NM_000018.4(ACADVL):c.1678+23C>T rs147546456
NM_000018.4(ACADVL):c.1679-5del rs1555528999
NM_000018.4(ACADVL):c.1733T>C (p.Met578Thr) rs375806217
NM_000018.4(ACADVL):c.1748C>G (p.Ser583Trp) rs1085307648
NM_000018.4(ACADVL):c.1825G>A (p.Glu609Lys) rs398123086
NM_000018.4(ACADVL):c.1828-4C>G rs184559206
NM_000018.4(ACADVL):c.1864C>T (p.Gln622Ter) rs1555529172
NM_000018.4(ACADVL):c.1894C>T (p.Arg632Cys) rs151254520
NM_000018.4(ACADVL):c.1923G>C (p.Leu641Phe) rs1452402269
NM_000018.4(ACADVL):c.204+5G>A rs958328801
NM_000018.4(ACADVL):c.205-5C>G rs768537914
NM_000018.4(ACADVL):c.205-8C>G rs774353448
NM_000018.4(ACADVL):c.227G>A (p.Gly76Glu) rs750043368
NM_000018.4(ACADVL):c.230T>C (p.Met77Thr) rs1555527718
NM_000018.4(ACADVL):c.278-8C>T rs1178133251
NM_000018.4(ACADVL):c.331_339del (p.Arg111_Phe113del) rs1555527820
NM_000018.4(ACADVL):c.439C>T (p.Pro147Ser) rs1032857886
NM_000018.4(ACADVL):c.481G>A (p.Ala161Thr) rs375284481
NM_000018.4(ACADVL):c.482C>T (p.Ala161Val) rs796051908
NM_000018.4(ACADVL):c.535G>T (p.Gly179Trp) rs796051909
NM_000018.4(ACADVL):c.538G>A (p.Ala180Thr) rs727503791
NM_000018.4(ACADVL):c.578G>A (p.Gly193Asp) rs1220348903
NM_000018.4(ACADVL):c.619T>C (p.Ser207Pro) rs768975918
NM_000018.4(ACADVL):c.62+6T>C rs1555527495
NM_000018.4(ACADVL):c.640T>G (p.Phe214Val) rs1192969297
NM_000018.4(ACADVL):c.739A>G (p.Lys247Glu) rs387906253
NM_000018.4(ACADVL):c.759_761del (p.Gly254del) rs1555528346
NM_000018.4(ACADVL):c.881G>A (p.Gly294Glu) rs200573371
NM_000018.4(ACADVL):c.898A>G (p.Met300Val) rs1026112888
NM_000018.4(ACADVL):c.944T>G (p.Val315Gly) rs1555528469

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