ClinVar Miner

List of variants in gene ACADVL reported as uncertain significance

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Gene type:
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Total variants: 199
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HGVS dbSNP
NM_000018.3(ACADVL):c.1679-5delG rs1555528999
NM_000018.3(ACADVL):c.878+5_878+8delGTGA rs886043503
NM_000018.4(ACADVL):c.*32T>G rs886053376
NM_000018.4(ACADVL):c.*53C>T rs535274747
NM_000018.4(ACADVL):c.*8del rs398123078
NM_000018.4(ACADVL):c.1001T>G (p.Met334Arg) rs398123079
NM_000018.4(ACADVL):c.1005C>A (p.His335Gln) rs753624994
NM_000018.4(ACADVL):c.1006A>G (p.Ile336Val) rs146369181
NM_000018.4(ACADVL):c.1009C>T (p.Leu337Phe) rs1567565656
NM_000018.4(ACADVL):c.1009_1011del (p.Leu337del) rs1315330884
NM_000018.4(ACADVL):c.100G>A (p.Gly34Ser)
NM_000018.4(ACADVL):c.1019G>T (p.Gly340Val) rs934797393
NM_000018.4(ACADVL):c.1024T>C (p.Phe342Leu) rs1356652354
NM_000018.4(ACADVL):c.1037C>T (p.Ala346Val) rs1303150138
NM_000018.4(ACADVL):c.1049G>C (p.Gly350Ala)
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.105_109dup (p.Arg37fs) rs1555527532
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.1076C>T (p.Ala359Val) rs539029862
NM_000018.4(ACADVL):c.1077G>A (p.Ala359=) rs779458466
NM_000018.4(ACADVL):c.1079T>C (p.Val360Ala)
NM_000018.4(ACADVL):c.1096C>T (p.Arg366Cys) rs771874163
NM_000018.4(ACADVL):c.109C>T (p.Arg37Trp) rs536992268
NM_000018.4(ACADVL):c.1103A>C (p.Gln368Pro) rs776063244
NM_000018.4(ACADVL):c.1127T>C (p.Phe376Ser) rs758928307
NM_000018.4(ACADVL):c.1153C>T (p.Arg385Trp) rs745832866
NM_000018.4(ACADVL):c.1182+2dup
NM_000018.4(ACADVL):c.1183-15A>G rs765390290
NM_000018.4(ACADVL):c.1183-2dup rs1555528721
NM_000018.4(ACADVL):c.1183-7A>G
NM_000018.4(ACADVL):c.1198G>A (p.Val400Met) rs149116708
NM_000018.4(ACADVL):c.1205C>T (p.Ala402Val) rs727503793
NM_000018.4(ACADVL):c.1217A>C (p.Gln406Pro) rs1384021857
NM_000018.4(ACADVL):c.121G>A (p.Ala41Thr)
NM_000018.4(ACADVL):c.1220G>C (p.Gly407Ala) rs904631654
NM_000018.4(ACADVL):c.1226C>T (p.Thr409Met) rs113994169
NM_000018.4(ACADVL):c.1246G>T (p.Ala416Ser) rs118204018
NM_000018.4(ACADVL):c.1253G>A (p.Ser418Asn) rs1555528737
NM_000018.4(ACADVL):c.1268C>T (p.Ser423Leu) rs1451455641
NM_000018.4(ACADVL):c.1269G>A (p.Ser423=)
NM_000018.4(ACADVL):c.1273G>A (p.Ala425Thr) rs138834083
NM_000018.4(ACADVL):c.1276G>A (p.Ala426Thr)
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.1291G>C (p.Asp431His)
NM_000018.4(ACADVL):c.1297T>C (p.Cys433Arg) rs886053374
NM_000018.4(ACADVL):c.129T>A (p.Gly43=) rs727503789
NM_000018.4(ACADVL):c.1313G>A (p.Gly438Glu) rs748450834
NM_000018.4(ACADVL):c.1316G>A (p.Gly439Asp) rs533055438
NM_000018.4(ACADVL):c.1328T>G (p.Met443Arg) rs886043236
NM_000018.4(ACADVL):c.1340G>A (p.Gly447Glu) rs1555528779
NM_000018.4(ACADVL):c.1345G>C (p.Glu449Gln) rs398123081
NM_000018.4(ACADVL):c.1360G>A (p.Asp454Asn) rs1419606204
NM_000018.4(ACADVL):c.1366C>T (p.Arg456Cys) rs794727111
NM_000018.4(ACADVL):c.1367G>A (p.Arg456His) rs794727112
NM_000018.4(ACADVL):c.1375C>T (p.Arg459Trp) rs766742117
NM_000018.4(ACADVL):c.1376G>C (p.Arg459Pro) rs751995154
NM_000018.4(ACADVL):c.138+2dup rs1555527548
NM_000018.4(ACADVL):c.1388G>A (p.Gly463Glu) rs200366828
NM_000018.4(ACADVL):c.139-3C>T rs1555527630
NM_000018.4(ACADVL):c.1391C>T (p.Thr464Ile) rs1555528796
NM_000018.4(ACADVL):c.1430G>A (p.Cys477Tyr) rs1555528803
NM_000018.4(ACADVL):c.1434+14T>A rs202217537
NM_000018.4(ACADVL):c.1434G>A (p.Met478Ile) rs775537775
NM_000018.4(ACADVL):c.1468G>C (p.Ala490Pro) rs759775666
NM_000018.4(ACADVL):c.1473A>G (p.Leu491=) rs150518187
NM_000018.4(ACADVL):c.1496G>C (p.Gly499Ala)
NM_000018.4(ACADVL):c.1532G>A (p.Arg511Gln) rs200771970
NM_000018.4(ACADVL):c.1532G>C (p.Arg511Pro) rs200771970
NM_000018.4(ACADVL):c.1533-4T>A rs369986567
NM_000018.4(ACADVL):c.1534C>T (p.Arg512Trp)
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.1581G>A (p.Pro527=) rs149436747
NM_000018.4(ACADVL):c.1591C>T (p.Arg531Trp) rs146379816
NM_000018.4(ACADVL):c.1600G>A (p.Glu534Lys) rs2230180
NM_000018.4(ACADVL):c.1613G>A (p.Arg538Gln) rs201350598
NM_000018.4(ACADVL):c.1613G>C (p.Arg538Pro) rs201350598
NM_000018.4(ACADVL):c.1616C>A (p.Ala539Asp) rs781613690
NM_000018.4(ACADVL):c.1617T>C (p.Ala539=) rs1555528948
NM_000018.4(ACADVL):c.1657A>C (p.Lys553Gln) rs1555528957
NM_000018.4(ACADVL):c.1678+23C>T rs147546456
NM_000018.4(ACADVL):c.1678+3_1678+6del
NM_000018.4(ACADVL):c.1678+4A>T rs1057518417
NM_000018.4(ACADVL):c.1699C>T (p.Arg567Trp) rs864321651
NM_000018.4(ACADVL):c.1700G>A (p.Arg567Gln) rs398123084
NM_000018.4(ACADVL):c.1711G>A (p.Gly571Arg) rs398123085
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.1754C>T (p.Ala585Val) rs374729641
NM_000018.4(ACADVL):c.1766T>C (p.Leu589Pro) rs1567569494
NM_000018.4(ACADVL):c.1803G>A (p.Met601Ile) rs201462718
NM_000018.4(ACADVL):c.180G>C (p.Leu60=) rs886053372
NM_000018.4(ACADVL):c.1820G>A (p.Cys607Tyr) rs200117742
NM_000018.4(ACADVL):c.1820G>C (p.Cys607Ser) rs200117742
NM_000018.4(ACADVL):c.1824C>T (p.Ile608=) rs146115467
NM_000018.4(ACADVL):c.1825G>A (p.Glu609Lys) rs398123086
NM_000018.4(ACADVL):c.1828-4C>G rs184559206
NM_000018.4(ACADVL):c.1835C>G (p.Ala612Gly) rs374898424
NM_000018.4(ACADVL):c.1839G>A (p.Arg613=) rs79125791
NM_000018.4(ACADVL):c.1844G>A (p.Arg615Gln) rs148584617
NM_000018.4(ACADVL):c.1864C>T (p.Gln622Ter) rs1555529172
NM_000018.4(ACADVL):c.1873C>G (p.Pro625Ala)
NM_000018.4(ACADVL):c.1878G>A (p.Trp626Ter) rs1555529186
NM_000018.4(ACADVL):c.1894C>T (p.Arg632Cys) rs151254520
NM_000018.4(ACADVL):c.189A>G (p.Lys63=) rs727503790
NM_000018.4(ACADVL):c.1923G>C (p.Leu641Phe) rs1452402269
NM_000018.4(ACADVL):c.1929G>C (p.Glu643Asp) rs1208010882
NM_000018.4(ACADVL):c.1932G>A (p.Arg644=) rs886053375
NM_000018.4(ACADVL):c.204+4G>C
NM_000018.4(ACADVL):c.204+5G>A rs958328801
NM_000018.4(ACADVL):c.205-5C>G rs768537914
NM_000018.4(ACADVL):c.205-7T>C rs760625298
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.271C>T (p.Pro91Ser) rs398123087
NM_000018.4(ACADVL):c.277+6G>T rs776422793
NM_000018.4(ACADVL):c.278-8C>T rs1178133251
NM_000018.4(ACADVL):c.278T>C (p.Val93Ala) rs886053373
NM_000018.4(ACADVL):c.286G>A (p.Glu96Lys)
NM_000018.4(ACADVL):c.294G>C (p.Gln98His) rs794727695
NM_000018.4(ACADVL):c.298C>G (p.Gln100Glu)
NM_000018.4(ACADVL):c.322C>G (p.Pro108Ala) rs886043235
NM_000018.4(ACADVL):c.325G>A (p.Val109Met) rs754207297
NM_000018.4(ACADVL):c.326T>A (p.Val109Glu) rs1555527815
NM_000018.4(ACADVL):c.331_339del (p.Arg111_Phe113del) rs1555527820
NM_000018.4(ACADVL):c.339C>A (p.Phe113Leu) rs750653177
NM_000018.4(ACADVL):c.340G>A (p.Glu114Lys) rs557260142
NM_000018.4(ACADVL):c.364A>G (p.Asn122Asp) rs1057520088
NM_000018.4(ACADVL):c.368A>G (p.Asp123Gly) rs1131691301
NM_000018.4(ACADVL):c.374T>C (p.Leu125Pro) rs1416443472
NM_000018.4(ACADVL):c.385G>A (p.Glu129Lys) rs1402849815
NM_000018.4(ACADVL):c.425T>C (p.Phe142Ser) rs398123088
NM_000018.4(ACADVL):c.427G>T (p.Gly143Cys) rs794727773
NM_000018.4(ACADVL):c.428G>A (p.Gly143Asp) rs1458941582
NM_000018.4(ACADVL):c.431T>C (p.Leu144Pro) rs1555527925
NM_000018.4(ACADVL):c.436G>C (p.Val146Leu) rs398123089
NM_000018.4(ACADVL):c.439C>T (p.Pro147Ser) rs1032857886
NM_000018.4(ACADVL):c.455G>A (p.Gly152Asp) rs794727772
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.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.535G>T (p.Gly179Trp) rs796051909
NM_000018.4(ACADVL):c.538G>A (p.Ala180Thr) rs727503791
NM_000018.4(ACADVL):c.542A>G (p.His181Arg) rs1425862331
NM_000018.4(ACADVL):c.575T>C (p.Phe192Ser) rs1555528189
NM_000018.4(ACADVL):c.578G>A (p.Gly193Asp) rs1220348903
NM_000018.4(ACADVL):c.605T>A (p.Leu202His) rs398123090
NM_000018.4(ACADVL):c.605T>C (p.Leu202Pro) rs398123090
NM_000018.4(ACADVL):c.619T>C (p.Ser207Pro) rs768975918
NM_000018.4(ACADVL):c.62+6T>C rs1555527495
NM_000018.4(ACADVL):c.623-8C>T rs144996066
NM_000018.4(ACADVL):c.636C>T (p.Ala212=) rs76547988
NM_000018.4(ACADVL):c.637G>A (p.Ala213Thr) rs140629318
NM_000018.4(ACADVL):c.637G>C (p.Ala213Pro) rs140629318
NM_000018.4(ACADVL):c.640T>G (p.Phe214Val) rs1192969297
NM_000018.4(ACADVL):c.652G>A (p.Glu218Lys) rs1432183079
NM_000018.4(ACADVL):c.678C>A (p.Ala226=) rs372114185
NM_000018.4(ACADVL):c.689C>T (p.Thr230Ile)
NM_000018.4(ACADVL):c.693T>A (p.Ser231=) rs77763289
NM_000018.4(ACADVL):c.713G>T (p.Gly238Val) rs886044100
NM_000018.4(ACADVL):c.734G>A (p.Gly245Glu)
NM_000018.4(ACADVL):c.736A>G (p.Ser246Gly) rs1555528320
NM_000018.4(ACADVL):c.739A>G (p.Lys247Glu) rs387906253
NM_000018.4(ACADVL):c.747G>C (p.Trp249Cys) rs141167669
NM_000018.4(ACADVL):c.751A>G (p.Ser251Gly) rs749159573
NM_000018.4(ACADVL):c.752+5C>T
NM_000018.4(ACADVL):c.753-11T>G rs1555528341
NM_000018.4(ACADVL):c.756T>A (p.Asn252Lys) rs143233413
NM_000018.4(ACADVL):c.757G>A (p.Gly253Arg) rs1555528345
NM_000018.4(ACADVL):c.759_761del (p.Gly254del) rs1555528346
NM_000018.4(ACADVL):c.787G>A (p.Ala263Thr) rs398123093
NM_000018.4(ACADVL):c.79C>T (p.Leu27Phe)
NM_000018.4(ACADVL):c.818G>C (p.Gly273Ala) rs150149784
NM_000018.4(ACADVL):c.826_849del (p.Lys276_Val283del) rs1555528367
NM_000018.4(ACADVL):c.829_831del (p.Glu277del) rs796051913
NM_000018.4(ACADVL):c.830_832AGA[1] (p.Lys278del) rs769280599
NM_000018.4(ACADVL):c.866G>A (p.Gly289Glu) rs778514103
NM_000018.4(ACADVL):c.86G>A (p.Gly29Glu) rs1247979958
NM_000018.4(ACADVL):c.881G>A (p.Gly294Glu) rs200573371
NM_000018.4(ACADVL):c.890_892AGA[2] (p.Lys299del) rs387906252
NM_000018.4(ACADVL):c.896A>G (p.Lys299Arg)
NM_000018.4(ACADVL):c.898A>G (p.Met300Val) rs1026112888
NM_000018.4(ACADVL):c.907A>G (p.Lys303Glu) rs369149696
NM_000018.4(ACADVL):c.944T>G (p.Val315Gly) rs1555528469
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
NM_000018.4(ACADVL):c.953C>T (p.Pro318Leu) rs201676770
NM_000018.4(ACADVL):c.95G>A (p.Arg32Gln)
NM_000018.4(ACADVL):c.963C>A (p.Asn321Lys)
NM_000018.4(ACADVL):c.969G>A (p.Leu323=) rs749734276
NM_000018.4(ACADVL):c.992A>C (p.Lys331Thr) rs727503792
NM_000018.4(ACADVL):c.994G>A (p.Val332Ile) rs775761275

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