List of variants in gene ACADVL reported as uncertain significance for not provided

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 97

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HGVS	dbSNP	gnomAD frequency
NM_000018.4(ACADVL):c.308A>G (p.Lys103Arg)	rs140566084	0.00391
NM_000018.4(ACADVL):c.1844G>A (p.Arg615Gln)	rs148584617	0.00244
NM_000018.4(ACADVL):c.818G>C (p.Gly273Ala)	rs150149784	0.00124
NM_000018.4(ACADVL):c.1567G>A (p.Gly523Arg)	rs139425622	0.00066
NM_000018.4(ACADVL):c.1591C>T (p.Arg531Trp)	rs146379816	0.00039
NM_000018.4(ACADVL):c.1894C>T (p.Arg632Cys)	rs151254520	0.00038
NM_000018.4(ACADVL):c.286G>A (p.Glu96Lys)	rs139427392	0.00035
NM_000018.4(ACADVL):c.587C>T (p.Ala196Val)	rs201370388	0.00034
NM_000018.4(ACADVL):c.1700G>A (p.Arg567Gln)	rs398123084	0.00014
NM_000018.4(ACADVL):c.1239A>G (p.Ile413Met)	rs143172658	0.00011
NM_000018.4(ACADVL):c.1005C>A (p.His335Gln)	rs753624994	0.00009
NM_000018.4(ACADVL):c.1273G>A (p.Ala425Thr)	rs138834083	0.00009
NM_000018.4(ACADVL):c.1733T>C (p.Met578Thr)	rs375806217	0.00009
NM_000018.4(ACADVL):c.1803G>A (p.Met601Ile)	rs201462718	0.00009
NM_000018.4(ACADVL):c.1434G>A (p.Met478Ile)	rs775537775	0.00006
NM_000018.4(ACADVL):c.947G>A (p.Arg316Gln)	rs147366714	0.00006
NM_000018.4(ACADVL):c.1754C>T (p.Ala585Val)	rs374729641	0.00005
NM_000018.4(ACADVL):c.1153C>T (p.Arg385Trp)	rs745832866	0.00004
NM_000018.4(ACADVL):c.866G>A (p.Gly289Glu)	rs778514103	0.00004
NM_000018.4(ACADVL):c.1605+7G>A	rs572010910	0.00003
NM_000018.4(ACADVL):c.1711G>A (p.Gly571Arg)	rs398123085	0.00003
NM_000018.4(ACADVL):c.1931G>A (p.Arg644Gln)	rs774762384	0.00003
NM_000018.4(ACADVL):c.521T>C (p.Val174Ala)	rs372684079	0.00003
NM_000018.4(ACADVL):c.992A>C (p.Lys331Thr)	rs727503792	0.00003
NM_000018.4(ACADVL):c.1024T>C (p.Phe342Leu)	rs1356652354	0.00002
NM_000018.4(ACADVL):c.1366C>T (p.Arg456Cys)	rs794727111	0.00002
NM_000018.4(ACADVL):c.485G>A (p.Arg162His)	rs754756970	0.00002
NM_000018.4(ACADVL):c.1001T>G (p.Met334Arg)	rs398123079	0.00001
NM_000018.4(ACADVL):c.1006A>G (p.Ile336Val)	rs146369181	0.00001
NM_000018.4(ACADVL):c.1133T>C (p.Leu378Pro)	rs2071314177	0.00001
NM_000018.4(ACADVL):c.1182+3G>T	rs376281637	0.00001
NM_000018.4(ACADVL):c.1316G>A (p.Gly439Asp)	rs533055438	0.00001
NM_000018.4(ACADVL):c.1345G>C (p.Glu449Gln)	rs398123081	0.00001
NM_000018.4(ACADVL):c.1532G>A (p.Arg511Gln)	rs200771970	0.00001
NM_000018.4(ACADVL):c.1535G>A (p.Arg512Gln)	rs1363658463	0.00001
NM_000018.4(ACADVL):c.1552G>A (p.Gly518Ser)	rs374507980	0.00001
NM_000018.4(ACADVL):c.1599C>T (p.Gly533=)	rs779770406	0.00001
NM_000018.4(ACADVL):c.1612C>T (p.Arg538Trp)	rs192904909	0.00001
NM_000018.4(ACADVL):c.1678+4A>T	rs1057518417	0.00001
NM_000018.4(ACADVL):c.1820G>A (p.Cys607Tyr)	rs200117742	0.00001
NM_000018.4(ACADVL):c.1825G>A (p.Glu609Lys)	rs398123086	0.00001
NM_000018.4(ACADVL):c.1929G>C (p.Glu643Asp)	rs1208010882	0.00001
NM_000018.4(ACADVL):c.322C>G (p.Pro108Ala)	rs886043235	0.00001
NM_000018.4(ACADVL):c.385G>A (p.Glu129Lys)	rs1402849815	0.00001
NM_000018.4(ACADVL):c.427G>T (p.Gly143Cys)	rs794727773	0.00001
NM_000018.4(ACADVL):c.428G>A (p.Gly143Asp)	rs1458941582	0.00001
NM_000018.4(ACADVL):c.538G>A (p.Ala180Thr)	rs727503791	0.00001
NM_000018.4(ACADVL):c.605T>C (p.Leu202Pro)	rs398123090	0.00001
NM_000018.4(ACADVL):c.628A>C (p.Thr210Pro)	rs775400380	0.00001
NM_000018.4(ACADVL):c.637G>C (p.Ala213Pro)	rs140629318	0.00001
NM_000018.4(ACADVL):c.694G>A (p.Ala232Thr)	rs746944448	0.00001
NM_000018.4(ACADVL):c.715A>G (p.Lys239Glu)	rs776331587	0.00001
NM_000018.4(ACADVL):c.879-16C>A	rs780626099	0.00001
NM_000018.4(ACADVL):c.881G>A (p.Gly294Glu)	rs200573371	0.00001
NM_000018.4(ACADVL):c.950T>C (p.Val317Ala)	rs398123095	0.00001
NM_000018.4(ACADVL):c.*8del	rs398123078
NM_000018.4(ACADVL):c.1009C>T (p.Leu337Phe)	rs1567565656
NM_000018.4(ACADVL):c.1022G>C (p.Arg341Thr)	rs1064793382
NM_000018.4(ACADVL):c.1052C>T (p.Thr351Ile)	rs796051911
NM_000018.4(ACADVL):c.1062CAT[1] (p.Ile356del)	rs754325237
NM_000018.4(ACADVL):c.1103A>C (p.Gln368Pro)	rs776063244
NM_000018.4(ACADVL):c.1205C>T (p.Ala402Val)	rs727503793
NM_000018.4(ACADVL):c.1243GCC[1] (p.Ala416del)
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.1328T>G (p.Met443Arg)	rs886043236
NM_000018.4(ACADVL):c.1367G>A (p.Arg456His)	rs794727112
NM_000018.4(ACADVL):c.1434+14T>A	rs202217537
NM_000018.4(ACADVL):c.1467T>G (p.Ser489Arg)	rs771117714
NM_000018.4(ACADVL):c.1537G>C (p.Ala513Pro)	rs2142987648
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.1673T>C (p.Ile558Thr)	rs1256129137
NM_000018.4(ACADVL):c.189A>G (p.Lys63=)	rs727503790
NM_000018.4(ACADVL):c.205-8_205-7delinsGC	rs2142965218
NM_000018.4(ACADVL):c.271C>T (p.Pro91Ser)	rs398123087
NM_000018.4(ACADVL):c.294G>C (p.Gln98His)	rs794727695
NM_000018.4(ACADVL):c.326T>A (p.Val109Glu)	rs1555527815
NM_000018.4(ACADVL):c.368A>G (p.Asp123Gly)	rs1131691301
NM_000018.4(ACADVL):c.425T>C (p.Phe142Ser)	rs398123088
NM_000018.4(ACADVL):c.436G>C (p.Val146Leu)	rs398123089
NM_000018.4(ACADVL):c.455G>A (p.Gly152Asp)	rs794727772
NM_000018.4(ACADVL):c.495G>T (p.Glu165Asp)	rs370169077
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.581C>T (p.Thr194Ile)	rs753444680
NM_000018.4(ACADVL):c.605T>A (p.Leu202His)	rs398123090
NM_000018.4(ACADVL):c.640T>G (p.Phe214Val)	rs1192969297
NM_000018.4(ACADVL):c.678C>A (p.Ala226=)	rs372114185
NM_000018.4(ACADVL):c.713G>T (p.Gly238Val)	rs886044100
NM_000018.4(ACADVL):c.732T>A (p.Asn244Lys)	rs1567564195
NM_000018.4(ACADVL):c.787G>A (p.Ala263Thr)	rs398123093
NM_000018.4(ACADVL):c.811G>A (p.Ala271Thr)	rs2142977919
NM_000018.4(ACADVL):c.830AGA[1] (p.Lys278del)	rs769280599
NM_000018.4(ACADVL):c.878+5_878+8del	rs886043503
NM_000018.4(ACADVL):c.956C>T (p.Ser319Leu)	rs149467828

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