ClinVar Miner

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

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 137
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_000384.3(APOB):c.7545C>T (p.Thr2515=) rs693 0.38722
NM_000384.3(APOB):c.2706C>T (p.Asn902=) rs1801700 0.03627
NM_000384.3(APOB):c.11904-7C>T rs12720851 0.03622
NM_000384.3(APOB):c.10737C>T (p.Thr3579=) rs12713554 0.02896
NM_000384.3(APOB):c.11808C>T (p.Ile3936=) rs12720852 0.01624
NM_000384.3(APOB):c.3509-10G>A rs12720770 0.01624
NM_000384.3(APOB):c.2604+15G>C rs72653066 0.00842
NM_000384.3(APOB):c.905-15C>G rs72653061 0.00554
NM_000384.3(APOB):c.3383G>A (p.Arg1128His) rs12713843 0.00356
NM_000384.3(APOB):c.7696G>A (p.Glu2566Lys) rs1801696 0.00305
NM_000384.3(APOB):c.8462C>T (p.Pro2821Leu) rs72653095 0.00267
NM_000384.3(APOB):c.13369G>A (p.Asp4457Asn) rs183812948 0.00250
NM_000384.3(APOB):c.1785C>G (p.Ser595=) rs139864087 0.00247
NM_000384.3(APOB):c.3843C>T (p.Ser1281=) rs72653079 0.00240
NM_000384.3(APOB):c.3150A>G (p.Thr1050=) rs72653072 0.00231
NM_000384.3(APOB):c.12803T>C (p.Met4268Thr) rs72654422 0.00222
NM_000384.3(APOB):c.7242A>C (p.Glu2414Asp) rs72653091 0.00222
NM_000384.3(APOB):c.8889C>T (p.Ile2963=) rs72653097 0.00213
NM_000384.3(APOB):c.11833A>G (p.Thr3945Ala) rs1801698 0.00212
NM_000384.3(APOB):c.7615G>A (p.Val2539Ile) rs148170480 0.00210
NM_000384.3(APOB):c.12766G>A (p.Glu4256Lys) rs61743313 0.00198
NM_000384.3(APOB):c.751G>A (p.Ala251Thr) rs61741625 0.00190
NM_000384.3(APOB):c.905-16A>C rs12720810 0.00172
NM_000384.3(APOB):c.11819C>T (p.Thr3940Met) rs72654416 0.00161
NM_000384.3(APOB):c.9294C>T (p.Tyr3098=) rs145777339 0.00139
NM_000384.3(APOB):c.12699G>A (p.Ser4233=) rs56675344 0.00136
NM_000384.3(APOB):c.2068-4T>A rs41291161 0.00108
NM_000384.3(APOB):c.7612C>T (p.Leu2538=) rs72653093 0.00108
NM_000384.3(APOB):c.4838G>C (p.Ser1613Thr) rs61742247 0.00093
NM_000384.3(APOB):c.13449G>A (p.Ala4483=) rs138421941 0.00092
NM_000384.3(APOB):c.3509-11C>T rs200768300 0.00091
NM_000384.3(APOB):c.12903C>T (p.Asp4301=) rs200145506 0.00090
NM_000384.3(APOB):c.13102C>G (p.Gln4368Glu) rs72654424 0.00080
NM_000384.3(APOB):c.4178C>T (p.Ala1393Val) rs143282164 0.00073
NM_000384.3(APOB):c.3740A>G (p.Tyr1247Cys) rs61741164 0.00071
NM_000384.3(APOB):c.895T>G (p.Phe299Val) rs72653060 0.00051
NM_000384.3(APOB):c.7152T>C (p.Val2384=) rs72653090 0.00041
NM_000384.3(APOB):c.8912A>C (p.Asn2971Thr) rs72653098 0.00026
NM_000384.3(APOB):c.10476T>A (p.Ile3492=) rs139929439 0.00021
NM_000384.3(APOB):c.11244G>A (p.Thr3748=) rs72654406 0.00020
NM_000384.3(APOB):c.11354C>T (p.Thr3785Ile) rs143710616 0.00019
NM_000384.3(APOB):c.12016G>A (p.Val4006Ile) rs183117027 0.00019
NM_000384.3(APOB):c.10385A>G (p.Tyr3462Cys) rs200305144 0.00014
NM_000384.3(APOB):c.244C>T (p.Leu82=) rs201658954 0.00014
NM_000384.3(APOB):c.11542G>A (p.Ala3848Thr) rs61743512 0.00012
NM_000384.3(APOB):c.8877G>A (p.Leu2959=) rs765899256 0.00012
NM_000384.3(APOB):c.3471T>C (p.Tyr1157=) rs201128198 0.00009
NM_000384.3(APOB):c.12318A>G (p.Arg4106=) rs375795401 0.00008
NM_000384.3(APOB):c.5622G>A (p.Gly1874=) rs144849403 0.00008
NM_000384.3(APOB):c.2938G>A (p.Ala980Thr) rs369310292 0.00007
NM_000384.3(APOB):c.7998A>G (p.Val2666=) rs1042006 0.00007
NM_000384.3(APOB):c.9491C>T (p.Thr3164Met) rs143269114 0.00007
NM_000384.3(APOB):c.10579C>T (p.Arg3527Trp) rs144467873 0.00006
NM_000384.3(APOB):c.11934C>T (p.Ile3978=) rs539824713 0.00006
NM_000384.3(APOB):c.4157G>A (p.Arg1386Gln) rs145007060 0.00006
NM_000384.3(APOB):c.8599C>T (p.Leu2867=) rs149430596 0.00006
NM_000384.3(APOB):c.3594C>T (p.Ser1198=) rs138243977 0.00005
NM_000384.3(APOB):c.1061A>G (p.Glu354Gly) rs149227065 0.00004
NM_000384.3(APOB):c.11303T>C (p.Ile3768Thr) rs376825639 0.00004
NM_000384.3(APOB):c.1400C>G (p.Ala467Gly) rs376602710 0.00004
NM_000384.3(APOB):c.2047G>T (p.Ala683Ser) rs761947252 0.00004
NM_000384.3(APOB):c.5022G>A (p.Glu1674=) rs367718499 0.00004
NM_000384.3(APOB):c.5705C>T (p.Pro1902Leu) rs368848646 0.00004
NM_000384.3(APOB):c.6201C>T (p.His2067=) rs143222685 0.00004
NM_000384.3(APOB):c.10056C>A (p.Thr3352=) rs369022661 0.00003
NM_000384.3(APOB):c.12021C>A (p.Gly4007=) rs145498491 0.00003
NM_000384.3(APOB):c.3034G>A (p.Glu1012Lys) rs575505383 0.00003
NM_000384.3(APOB):c.5028C>T (p.Gly1676=) rs201446451 0.00003
NM_000384.3(APOB):c.543C>T (p.Thr181=) rs778023021 0.00003
NM_000384.3(APOB):c.6513A>G (p.Leu2171=) rs547853968 0.00003
NM_000384.3(APOB):c.13399G>A (p.Ala4467Thr) rs1407600482 0.00001
NM_000384.3(APOB):c.2556A>C (p.Gly852=) rs778199079 0.00001
NM_000384.3(APOB):c.5617G>A (p.Ala1873Thr) rs750451480 0.00001
NM_000384.3(APOB):c.6390T>C (p.Asn2130=) rs570798466 0.00001
NM_000384.3(APOB):c.819-10T>G rs749762235 0.00001
NM_000384.3(APOB):c.9501A>G (p.Gln3167=) rs533171453 0.00001
NM_000384.3(APOB):c.10186G>A (p.Ala3396Thr) rs1553383017
NM_000384.3(APOB):c.10580G>A (p.Arg3527Gln)
NM_000384.3(APOB):c.10701G>T (p.Thr3567=) rs12713558
NM_000384.3(APOB):c.10913G>A (p.Arg3638Gln)
NM_000384.3(APOB):c.11401T>A (p.Ser3801Thr)
NM_000384.3(APOB):c.11477C>T (p.Thr3826Met)
NM_000384.3(APOB):c.11761G>A (p.Val3921Ile)
NM_000384.3(APOB):c.12053A>G (p.Asp4018Gly) rs771555558
NM_000384.3(APOB):c.12404G>T (p.Ser4135Ile)
NM_000384.3(APOB):c.12460G>T (p.Glu4154Ter)
NM_000384.3(APOB):c.12541G>A (p.Glu4181Lys)
NM_000384.3(APOB):c.12697T>A (p.Ser4233Thr)
NM_000384.3(APOB):c.12809G>C (p.Arg4270Thr)
NM_000384.3(APOB):c.13013G>A (p.Ser4338Asn)
NM_000384.3(APOB):c.13028_13029del (p.Tyr4343fs) rs760832994
NM_000384.3(APOB):c.13070A>G (p.His4357Arg)
NM_000384.3(APOB):c.1310G>A (p.Arg437His)
NM_000384.3(APOB):c.13441G>A (p.Ala4481Thr)
NM_000384.3(APOB):c.13451C>T (p.Thr4484Met)
NM_000384.3(APOB):c.1468C>T (p.Arg490Trp) rs771541567
NM_000384.3(APOB):c.1594C>T (p.Arg532Trp)
NM_000384.3(APOB):c.1853C>T (p.Ala618Val)
NM_000384.3(APOB):c.2188G>A (p.Val730Ile)
NM_000384.3(APOB):c.2863C>T (p.Pro955Ser)
NM_000384.3(APOB):c.293C>T (p.Thr98Ile)
NM_000384.3(APOB):c.3000-1G>A
NM_000384.3(APOB):c.307T>C (p.Tyr103His)
NM_000384.3(APOB):c.3122-6G>A rs72653071
NM_000384.3(APOB):c.3122-6G>T rs72653071
NM_000384.3(APOB):c.3201G>A (p.Pro1067=) rs200281277
NM_000384.3(APOB):c.3337G>C (p.Asp1113His)
NM_000384.3(APOB):c.3427C>T (p.Pro1143Ser)
NM_000384.3(APOB):c.444T>C (p.Asp148=)
NM_000384.3(APOB):c.5066G>A (p.Arg1689His)
NM_000384.3(APOB):c.5163C>T (p.Val1721=) rs536182427
NM_000384.3(APOB):c.5741A>G (p.Asn1914Ser)
NM_000384.3(APOB):c.5768A>G (p.His1923Arg)
NM_000384.3(APOB):c.5815G>A (p.Ala1939Thr)
NM_000384.3(APOB):c.5941T>G (p.Trp1981Gly)
NM_000384.3(APOB):c.6057A>G (p.Leu2019=)
NM_000384.3(APOB):c.6063C>G (p.Asp2021Glu) rs556582055
NM_000384.3(APOB):c.6231G>A (p.Leu2077=)
NM_000384.3(APOB):c.6636TGA[1] (p.Asp2213del) rs541497967
NM_000384.3(APOB):c.677C>T (p.Ala226Val)
NM_000384.3(APOB):c.693+7C>T
NM_000384.3(APOB):c.6936_6937inv (p.Ile2313Val)
NM_000384.3(APOB):c.7367C>A (p.Ala2456Asp)
NM_000384.3(APOB):c.7832C>G (p.Thr2611Ser) rs138790085
NM_000384.3(APOB):c.8216C>T (p.Pro2739Leu)
NM_000384.3(APOB):c.8226G>A (p.Gln2742=) rs376773500
NM_000384.3(APOB):c.8363G>T (p.Gly2788Val) rs534116066
NM_000384.3(APOB):c.8529G>T (p.Met2843Ile)
NM_000384.3(APOB):c.8757A>G (p.Ile2919Met)
NM_000384.3(APOB):c.9204A>C (p.Ile3068=)
NM_000384.3(APOB):c.9242G>A (p.Ser3081Asn) rs72653100
NM_000384.3(APOB):c.9242G>C (p.Ser3081Thr) rs72653100
NM_000384.3(APOB):c.9384T>A (p.Ile3128=)
NM_000384.3(APOB):c.9502T>A (p.Ser3168Thr) rs761382742
NM_000384.3(APOB):c.9715C>T (p.His3239Tyr) rs755547544
NM_000384.3(APOB):c.9835A>G (p.Ser3279Gly)
NM_000384.3(APOB):c.9880T>C (p.Ser3294Pro)

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.