ClinVar Miner

List of variants in gene APOB reported as uncertain significance by Fulgent Genetics, Fulgent Genetics

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 211
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_000384.3(APOB):c.9322G>A (p.Glu3108Lys) rs140240214 0.00033
NM_000384.3(APOB):c.10708C>T (p.His3570Tyr) rs201736972 0.00021
NM_000384.3(APOB):c.12959T>C (p.Met4320Thr) rs377127458 0.00020
NM_000384.3(APOB):c.3724T>A (p.Ser1242Thr) rs200261177 0.00020
NM_000384.3(APOB):c.13181T>C (p.Val4394Ala) rs12720843 0.00017
NM_000384.3(APOB):c.6969T>A (p.Asn2323Lys) rs138118085 0.00016
NM_000384.3(APOB):c.7721C>T (p.Ala2574Val) rs150843941 0.00016
NM_000384.3(APOB):c.8882A>G (p.Asn2961Ser) rs142756262 0.00016
NM_000384.3(APOB):c.4970C>T (p.Thr1657Met) rs144239254 0.00015
NM_000384.3(APOB):c.7577T>C (p.Met2526Thr) rs373272476 0.00015
NM_000384.3(APOB):c.2914G>A (p.Gly972Ser) rs199893862 0.00014
NM_000384.3(APOB):c.6941T>C (p.Leu2314Pro) rs372035579 0.00014
NM_000384.3(APOB):c.1010T>A (p.Ile337Asn) rs148126873 0.00013
NM_000384.3(APOB):c.2611G>A (p.Ala871Thr) rs144622446 0.00013
NM_000384.3(APOB):c.3049A>C (p.Ser1017Arg) rs149323475 0.00013
NM_000384.3(APOB):c.2258G>A (p.Gly753Glu) rs148502464 0.00012
NM_000384.3(APOB):c.5434G>T (p.Gly1812Trp) rs140174653 0.00012
NM_000384.3(APOB):c.4111G>A (p.Ala1371Thr) rs780170292 0.00011
NM_000384.3(APOB):c.5650A>G (p.Asn1884Asp) rs146472818 0.00011
NM_000384.3(APOB):c.574G>A (p.Val192Ile) rs200662943 0.00011
NM_000384.3(APOB):c.7006G>A (p.Ala2336Thr) rs146888928 0.00011
NM_000384.3(APOB):c.7759G>C (p.Val2587Leu) rs375855688 0.00011
NM_000384.3(APOB):c.8855G>T (p.Gly2952Val) rs369472561 0.00011
NM_000384.3(APOB):c.890G>A (p.Arg297His) rs147223101 0.00011
NM_000384.3(APOB):c.1316G>A (p.Arg439Gln) rs61742990 0.00010
NM_000384.3(APOB):c.2123A>G (p.Gln708Arg) rs371190827 0.00010
NM_000384.3(APOB):c.5137G>T (p.Ala1713Ser) rs769789232 0.00010
NM_000384.3(APOB):c.10295A>G (p.Gln3432Arg) rs759043889 0.00009
NM_000384.3(APOB):c.10700C>T (p.Thr3567Met) rs368278927 0.00009
NM_000384.3(APOB):c.11816G>A (p.Gly3939Asp) rs142828185 0.00009
NM_000384.3(APOB):c.3972G>T (p.Lys1324Asn) rs775070656 0.00009
NM_000384.3(APOB):c.2312C>T (p.Pro771Leu) rs200524554 0.00007
NM_000384.3(APOB):c.5600G>A (p.Arg1867Gln) rs371337253 0.00007
NM_000384.3(APOB):c.6655C>T (p.Arg2219Cys) rs141641980 0.00007
NM_000384.3(APOB):c.9491C>T (p.Thr3164Met) rs143269114 0.00007
NM_000384.3(APOB):c.12677C>T (p.Thr4226Met) rs371177562 0.00006
NM_000384.3(APOB):c.12731C>G (p.Ser4244Cys) rs1052000878 0.00006
NM_000384.3(APOB):c.3246A>C (p.Glu1082Asp) rs371987644 0.00006
NM_000384.3(APOB):c.3449T>A (p.Met1150Lys) rs146223051 0.00006
NM_000384.3(APOB):c.4421A>G (p.Lys1474Arg) rs759246439 0.00006
NM_000384.3(APOB):c.5387C>G (p.Thr1796Ser) rs529168934 0.00006
NM_000384.3(APOB):c.5560G>A (p.Asp1854Asn) rs138005301 0.00006
NM_000384.3(APOB):c.5734A>T (p.Asn1912Tyr) rs186480094 0.00006
NM_000384.3(APOB):c.6019G>A (p.Val2007Met) rs145424390 0.00006
NM_000384.3(APOB):c.7094C>T (p.Ala2365Val) rs200034452 0.00006
NM_000384.3(APOB):c.8198T>C (p.Val2733Ala) rs771792572 0.00006
NM_000384.3(APOB):c.9317A>G (p.Asn3106Ser) rs546747242 0.00006
NM_000384.3(APOB):c.9407G>A (p.Arg3136His) rs199590149 0.00006
NM_000384.3(APOB):c.9493A>G (p.Thr3165Ala) rs149166048 0.00006
NM_000384.3(APOB):c.11018A>G (p.Lys3673Arg) rs374411400 0.00005
NM_000384.3(APOB):c.2657A>G (p.Asn886Ser) rs183398286 0.00005
NM_000384.3(APOB):c.6125T>C (p.Met2042Thr) rs371224295 0.00005
NM_000384.3(APOB):c.7057C>A (p.Gln2353Lys) rs758067709 0.00005
NM_000384.3(APOB):c.7336G>A (p.Val2446Met) rs777259835 0.00005
NM_000384.3(APOB):c.7655A>G (p.Asp2552Gly) rs779100523 0.00005
NM_000384.3(APOB):c.8297C>T (p.Ser2766Phe) rs1225631813 0.00005
NM_000384.3(APOB):c.9448T>C (p.Phe3150Leu) rs185224477 0.00005
NM_000384.3(APOB):c.10276G>A (p.Ala3426Thr) rs753767897 0.00004
NM_000384.3(APOB):c.11303T>C (p.Ile3768Thr) rs376825639 0.00004
NM_000384.3(APOB):c.11503A>C (p.Ile3835Leu) rs776119459 0.00004
NM_000384.3(APOB):c.11840G>A (p.Gly3947Glu) rs770531319 0.00004
NM_000384.3(APOB):c.12136C>T (p.Arg4046Trp) rs200222843 0.00004
NM_000384.3(APOB):c.12443C>A (p.Ala4148Asp) rs756476242 0.00004
NM_000384.3(APOB):c.12536C>T (p.Thr4179Ile) rs370180297 0.00004
NM_000384.3(APOB):c.1400C>G (p.Ala467Gly) rs376602710 0.00004
NM_000384.3(APOB):c.1753C>A (p.Gln585Lys) rs140101603 0.00004
NM_000384.3(APOB):c.1910A>G (p.Tyr637Cys) rs766573431 0.00004
NM_000384.3(APOB):c.1951G>C (p.Ala651Pro) rs377179209 0.00004
NM_000384.3(APOB):c.3220G>A (p.Gly1074Arg) rs72653074 0.00004
NM_000384.3(APOB):c.4298C>T (p.Ser1433Leu) rs200708197 0.00004
NM_000384.3(APOB):c.4441G>A (p.Val1481Ile) rs748985164 0.00004
NM_000384.3(APOB):c.6100A>G (p.Ile2034Val) rs200339216 0.00004
NM_000384.3(APOB):c.8635A>T (p.Asn2879Tyr) rs200367807 0.00004
NM_000384.3(APOB):c.10262T>C (p.Met3421Thr) rs755119833 0.00003
NM_000384.3(APOB):c.13448C>T (p.Ala4483Val) rs147416761 0.00003
NM_000384.3(APOB):c.2170G>T (p.Gly724Cys) rs143425834 0.00003
NM_000384.3(APOB):c.3851G>A (p.Arg1284Gln) rs372154910 0.00003
NM_000384.3(APOB):c.4352G>T (p.Gly1451Val) rs777471630 0.00003
NM_000384.3(APOB):c.5164G>A (p.Asp1722Asn) rs757793421 0.00003
NM_000384.3(APOB):c.598G>A (p.Ala200Thr) rs763878189 0.00003
NM_000384.3(APOB):c.5991T>A (p.Asp1997Glu) rs768045701 0.00003
NM_000384.3(APOB):c.655C>T (p.Arg219Cys) rs145661815 0.00003
NM_000384.3(APOB):c.6731G>A (p.Ser2244Asn) rs146333152 0.00003
NM_000384.3(APOB):c.6794A>C (p.Lys2265Thr) rs759255307 0.00003
NM_000384.3(APOB):c.7565G>A (p.Arg2522Gln) rs781243278 0.00003
NM_000384.3(APOB):c.7939A>C (p.Thr2647Pro) rs748143305 0.00003
NM_000384.3(APOB):c.8258C>G (p.Pro2753Arg) rs765290152 0.00003
NM_000384.3(APOB):c.8299C>T (p.Pro2767Ser) rs138465008 0.00003
NM_000384.3(APOB):c.8693T>C (p.Leu2898Pro) rs376974746 0.00003
NM_000384.3(APOB):c.8840G>C (p.Ser2947Thr) rs183475426 0.00003
NM_000384.3(APOB):c.889C>T (p.Arg297Cys) rs766376456 0.00003
NM_000384.3(APOB):c.9077A>T (p.Asn3026Ile) rs770981667 0.00003
NM_000384.3(APOB):c.11087T>C (p.Ile3696Thr) rs370096275 0.00002
NM_000384.3(APOB):c.11309T>G (p.Ile3770Ser) rs199954127 0.00002
NM_000384.3(APOB):c.11339C>T (p.Ala3780Val) rs755025293 0.00002
NM_000384.3(APOB):c.12698C>T (p.Ser4233Leu) rs377125320 0.00002
NM_000384.3(APOB):c.12779A>G (p.His4260Arg) rs781061676 0.00002
NM_000384.3(APOB):c.12851T>C (p.Phe4284Ser) rs750204106 0.00002
NM_000384.3(APOB):c.12890G>A (p.Arg4297His) rs375701380 0.00002
NM_000384.3(APOB):c.13130T>C (p.Ile4377Thr) rs778174655 0.00002
NM_000384.3(APOB):c.13463T>C (p.Ile4488Thr) rs374389311 0.00002
NM_000384.3(APOB):c.1595G>A (p.Arg532Gln) rs753831464 0.00002
NM_000384.3(APOB):c.2115T>G (p.Phe705Leu) rs747520197 0.00002
NM_000384.3(APOB):c.2203G>A (p.Val735Met) rs542107305 0.00002
NM_000384.3(APOB):c.2821A>T (p.Thr941Ser) rs748256431 0.00002
NM_000384.3(APOB):c.2999+8A>G rs752443893 0.00002
NM_000384.3(APOB):c.3271A>G (p.Arg1091Gly) rs368122382 0.00002
NM_000384.3(APOB):c.3676G>A (p.Val1226Met) rs138681343 0.00002
NM_000384.3(APOB):c.3828C>A (p.Asn1276Lys) rs199966747 0.00002
NM_000384.3(APOB):c.3935T>C (p.Met1312Thr) rs763989940 0.00002
NM_000384.3(APOB):c.4181A>G (p.Asp1394Gly) rs769694008 0.00002
NM_000384.3(APOB):c.4279C>T (p.Arg1427Cys) rs759979553 0.00002
NM_000384.3(APOB):c.4724A>G (p.Asn1575Ser) rs777879292 0.00002
NM_000384.3(APOB):c.4850G>A (p.Gly1617Glu) rs146341569 0.00002
NM_000384.3(APOB):c.4928C>T (p.Ala1643Val) rs1008238083 0.00002
NM_000384.3(APOB):c.5038G>T (p.Ala1680Ser) rs372282063 0.00002
NM_000384.3(APOB):c.544G>A (p.Val182Met) rs769838164 0.00002
NM_000384.3(APOB):c.5580G>T (p.Gln1860His) rs199585500 0.00002
NM_000384.3(APOB):c.7727G>A (p.Arg2576His) rs759057929 0.00002
NM_000384.3(APOB):c.9095C>A (p.Thr3032Asn) rs754332101 0.00002
NM_000384.3(APOB):c.10025C>T (p.Ser3342Phe) rs267599180 0.00001
NM_000384.3(APOB):c.1004T>C (p.Leu335Pro) rs759295942 0.00001
NM_000384.3(APOB):c.10261A>G (p.Met3421Val) rs1371028457 0.00001
NM_000384.3(APOB):c.10270T>C (p.Ser3424Pro) rs1425159052 0.00001
NM_000384.3(APOB):c.10314G>T (p.Met3438Ile) rs761164094 0.00001
NM_000384.3(APOB):c.1077T>G (p.Ser359Arg) rs752605091 0.00001
NM_000384.3(APOB):c.11078C>A (p.Thr3693Asn) rs776068398 0.00001
NM_000384.3(APOB):c.11374C>T (p.Pro3792Ser) rs767327489 0.00001
NM_000384.3(APOB):c.12025G>A (p.Val4009Met) rs140424976 0.00001
NM_000384.3(APOB):c.12122C>G (p.Thr4041Ser) rs776875782 0.00001
NM_000384.3(APOB):c.1216C>T (p.Leu406Phe) rs1663905539 0.00001
NM_000384.3(APOB):c.12340T>C (p.Trp4114Arg) rs750904831 0.00001
NM_000384.3(APOB):c.12635C>G (p.Thr4212Ser) rs201208445 0.00001
NM_000384.3(APOB):c.12739C>T (p.Gln4247Ter) rs907126709 0.00001
NM_000384.3(APOB):c.12889C>T (p.Arg4297Cys) rs761260344 0.00001
NM_000384.3(APOB):c.12977T>A (p.Ile4326Asn) rs763668912 0.00001
NM_000384.3(APOB):c.13319T>C (p.Val4440Ala) rs953483853 0.00001
NM_000384.3(APOB):c.1331C>T (p.Ala444Val) rs769425660 0.00001
NM_000384.3(APOB):c.1904G>A (p.Arg635Gln) rs202001155 0.00001
NM_000384.3(APOB):c.2144T>G (p.Val715Gly) rs1663743872 0.00001
NM_000384.3(APOB):c.2333G>A (p.Arg778His) rs201595604 0.00001
NM_000384.3(APOB):c.2335A>G (p.Ile779Val) rs763559077 0.00001
NM_000384.3(APOB):c.2414C>G (p.Thr805Ser) rs1291440333 0.00001
NM_000384.3(APOB):c.2605-6T>A rs1558570194 0.00001
NM_000384.3(APOB):c.2676G>A (p.Pro892=) rs759072451 0.00001
NM_000384.3(APOB):c.2849C>T (p.Thr950Met) rs187506285 0.00001
NM_000384.3(APOB):c.2864C>T (p.Pro955Leu) rs763052786 0.00001
NM_000384.3(APOB):c.3046G>C (p.Val1016Leu) rs770892328 0.00001
NM_000384.3(APOB):c.3147G>C (p.Met1049Ile) rs556469321 0.00001
NM_000384.3(APOB):c.3979G>A (p.Gly1327Arg) rs760203474 0.00001
NM_000384.3(APOB):c.3997C>G (p.Arg1333Gly) rs121918383 0.00001
NM_000384.3(APOB):c.4156C>T (p.Arg1386Trp) rs201270852 0.00001
NM_000384.3(APOB):c.460C>G (p.Leu154Val) rs914357651 0.00001
NM_000384.3(APOB):c.5203G>A (p.Gly1735Arg) rs1173916995 0.00001
NM_000384.3(APOB):c.5617G>A (p.Ala1873Thr) rs750451480 0.00001
NM_000384.3(APOB):c.6092G>C (p.Ser2031Thr) rs776946940 0.00001
NM_000384.3(APOB):c.638A>T (p.Asp213Val) rs370711366 0.00001
NM_000384.3(APOB):c.6698T>C (p.Ile2233Thr) rs1176839033 0.00001
NM_000384.3(APOB):c.6764A>C (p.Lys2255Thr) rs1249838546 0.00001
NM_000384.3(APOB):c.679C>G (p.Leu227Val) rs146880648 0.00001
NM_000384.3(APOB):c.7603T>C (p.Tyr2535His) rs146593015 0.00001
NM_000384.3(APOB):c.7717T>G (p.Trp2573Gly) rs763937444 0.00001
NM_000384.3(APOB):c.7979C>T (p.Ser2660Phe) rs1408828737 0.00001
NM_000384.3(APOB):c.8851G>A (p.Glu2951Lys) rs755952082 0.00001
NM_000384.3(APOB):c.9467C>A (p.Thr3156Lys) rs747569141 0.00001
NM_000384.3(APOB):c.9633C>A (p.Asn3211Lys) rs748318755 0.00001
NM_000384.3(APOB):c.9692A>G (p.Asp3231Gly) rs778780703 0.00001
NM_000384.3(APOB):c.9815A>G (p.Tyr3272Cys) rs1220960430 0.00001
NM_000384.3(APOB):c.10324C>A (p.Gln3442Lys) rs1663143963
NM_000384.3(APOB):c.10571A>C (p.Lys3524Thr) rs750035232
NM_000384.3(APOB):c.10724G>A (p.Gly3575Asp) rs1418775778
NM_000384.3(APOB):c.10727T>G (p.Leu3576Arg) rs1663130726
NM_000384.3(APOB):c.10811C>A (p.Ala3604Glu) rs776815102
NM_000384.3(APOB):c.11010G>C (p.Arg3670Ser) rs148127628
NM_000384.3(APOB):c.11088T>G (p.Ile3696Met) rs1663116627
NM_000384.3(APOB):c.11744C>T (p.Ser3915Phe) rs201990496
NM_000384.3(APOB):c.12005C>T (p.Ala4002Val) rs369364335
NM_000384.3(APOB):c.12309G>C (p.Lys4103Asn) rs574791609
NM_000384.3(APOB):c.12443_12444delinsAA (p.Ala4148Glu) rs1558559244
NM_000384.3(APOB):c.12824A>C (p.Asp4275Ala)
NM_000384.3(APOB):c.13238del (p.Asn4413fs) rs758853340
NM_000384.3(APOB):c.13320del (p.Glu4441fs) rs750076573
NM_000384.3(APOB):c.1385A>G (p.Glu462Gly) rs1558573118
NM_000384.3(APOB):c.1400C>T (p.Ala467Val) rs376602710
NM_000384.3(APOB):c.1497G>T (p.Met499Ile) rs1663829713
NM_000384.3(APOB):c.1568T>C (p.Ile523Thr) rs781234577
NM_000384.3(APOB):c.1784C>T (p.Ser595Phe) rs1047759477
NM_000384.3(APOB):c.2482C>T (p.His828Tyr) rs1663667473
NM_000384.3(APOB):c.3365G>T (p.Gly1122Val) rs1366616257
NM_000384.3(APOB):c.3847G>T (p.Gly1283Cys) rs2103361101
NM_000384.3(APOB):c.3850C>T (p.Arg1284Trp)
NM_000384.3(APOB):c.400G>A (p.Ala134Thr) rs368321279
NM_000384.3(APOB):c.5069T>A (p.Phe1690Tyr) rs751059071
NM_000384.3(APOB):c.5689C>T (p.Arg1897Cys) rs189341276
NM_000384.3(APOB):c.5983G>A (p.Asp1995Asn) rs917338225
NM_000384.3(APOB):c.6063C>G (p.Asp2021Glu) rs556582055
NM_000384.3(APOB):c.6161T>G (p.Ile2054Ser) rs538245770
NM_000384.3(APOB):c.6417G>C (p.Lys2139Asn) rs1558564270
NM_000384.3(APOB):c.6530A>C (p.Tyr2177Ser) rs1199919734
NM_000384.3(APOB):c.656G>T (p.Arg219Leu) rs201606169
NM_000384.3(APOB):c.695C>A (p.Thr232Asn) rs756001082
NM_000384.3(APOB):c.7540G>A (p.Glu2514Lys) rs1216733455
NM_000384.3(APOB):c.7726C>T (p.Arg2576Cys) rs767146440
NM_000384.3(APOB):c.8129A>T (p.Asp2710Val) rs771882254
NM_000384.3(APOB):c.8226G>T (p.Gln2742His) rs376773500
NM_000384.3(APOB):c.8375C>G (p.Ser2792Cys) rs368776368
NM_000384.3(APOB):c.8702C>G (p.Ser2901Cys) rs1663202923
NM_000384.3(APOB):c.8794G>A (p.Ala2932Thr) rs2103353864
NM_000384.3(APOB):c.9221A>G (p.Tyr3074Cys) rs372902533
NM_000384.3(APOB):c.9457T>C (p.Trp3153Arg) rs761484953
NM_000384.3(APOB):c.952C>A (p.Pro318Thr) rs758678209

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.