ClinVar Miner

List of variants in gene APOB reported by Robarts Research Institute,Western University

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 129
Download table as spreadsheet
HGVS dbSNP
NM_000384.3(APOB):c.10061C>G (p.Ala3354Gly) rs61742331
NM_000384.3(APOB):c.10131G>A (p.Leu3377=) rs1799812
NM_000384.3(APOB):c.10294C>G (p.Gln3432Glu) rs1042023
NM_000384.3(APOB):c.10367C>T (p.Ser3456Phe) rs1217782046
NM_000384.3(APOB):c.10371C>T (p.Ser3457=) rs139891446
NM_000384.3(APOB):c.10508C>T (p.Ser3503Leu) rs375284245
NM_000384.3(APOB):c.10579C>T (p.Arg3527Trp) rs144467873
NM_000384.3(APOB):c.10580G>A (p.Arg3527Gln) rs5742904
NM_000384.3(APOB):c.1061A>G (p.Glu354Gly) rs149227065
NM_000384.3(APOB):c.10701G>A (p.Thr3567=) rs12713558
NM_000384.3(APOB):c.10737C>T (p.Thr3579=) rs12713554
NM_000384.3(APOB):c.10740C>T (p.Asn3580=) rs150312765
NM_000384.3(APOB):c.10780T>C (p.Trp3594Arg) rs61744288
NM_000384.3(APOB):c.11356C>T (p.Leu3786Phe) rs571485213
NM_000384.3(APOB):c.11401T>A (p.Ser3801Thr) rs12713540
NM_000384.3(APOB):c.11477C>T (p.Thr3826Met) rs61744153
NM_000384.3(APOB):c.11509G>T (p.Ala3837Ser) rs1389480980
NM_000384.3(APOB):c.11808C>T (p.Ile3936=) rs12720852
NM_000384.3(APOB):c.11833A>G (p.Thr3945Ala) rs1801698
NM_000384.3(APOB):c.11904-7C>T rs12720851
NM_000384.3(APOB):c.11934C>T (p.Ile3978=) rs539824713
NM_000384.3(APOB):c.11965C>T (p.Arg3989Cys) rs150713761
NM_000384.3(APOB):c.1198C>T (p.Arg400Cys) rs778866803
NM_000384.3(APOB):c.12252T>C (p.Tyr4084=) rs138157751
NM_000384.3(APOB):c.12310C>A (p.Leu4104Met) rs199668351
NM_000384.3(APOB):c.12318A>G (p.Arg4106=) rs375795401
NM_000384.3(APOB):c.12343G>A (p.Val4115Ile) rs765681925
NM_000384.3(APOB):c.12382G>A (p.Val4128Met) rs1801703
NM_000384.3(APOB):c.12697T>A (p.Ser4233Thr) rs61743299
NM_000384.3(APOB):c.12794T>C (p.Val4265Ala) rs61743502
NM_000384.3(APOB):c.12809G>C (p.Arg4270Thr) rs1801702
NM_000384.3(APOB):c.12940A>G (p.Ile4314Val) rs72654423
NM_000384.3(APOB):c.13116A>G (p.Gln4372=) rs755500550
NM_000384.3(APOB):c.13160A>T (p.Glu4387Val) rs150412734
NM_000384.3(APOB):c.13302C>T (p.Ser4434=) rs144040999
NM_000384.3(APOB):c.13451C>T (p.Thr4484Met) rs12713450
NM_000384.3(APOB):c.13452G>A (p.Thr4484=) rs200374122
NM_000384.3(APOB):c.13477_13479CAG[1] (p.Gln4494del) rs562574661
NM_000384.3(APOB):c.1353-12C>T rs76202659
NM_000384.3(APOB):c.1402A>G (p.Asn468Asp) rs886804701
NM_000384.3(APOB):c.1470+15T>C rs185550846
NM_000384.3(APOB):c.1493C>T (p.Thr498Ile) rs758928147
NM_000384.3(APOB):c.1594C>T (p.Arg532Trp) rs13306194
NM_000384.3(APOB):c.1617+7T>C rs374552390
NM_000384.3(APOB):c.1618-13C>T rs1553386146
NM_000384.3(APOB):c.1734C>T (p.Val578=) rs1553386125
NM_000384.3(APOB):c.1773C>T (p.Asn591=) rs1553386116
NM_000384.3(APOB):c.1785C>G (p.Ser595=) rs139864087
NM_000384.3(APOB):c.2068-4T>A rs41291161
NM_000384.3(APOB):c.2222C>A (p.Thr741Asn) rs12714192
NM_000384.3(APOB):c.2308G>A (p.Val770Ile) rs1415675587
NM_000384.3(APOB):c.2604+15G>C rs72653066
NM_000384.3(APOB):c.2630C>T (p.Pro877Leu) rs12714097
NM_000384.3(APOB):c.2950G>A (p.Ala984Thr) rs752149683
NM_000384.3(APOB):c.2968G>A (p.Ala990Thr) rs139434026
NM_000384.3(APOB):c.2981C>T (p.Pro994Leu) rs41288783
NM_000384.3(APOB):c.3051C>T (p.Ser1017=) rs558838327
NM_000384.3(APOB):c.3052G>A (p.Ala1018Thr) rs149357946
NM_000384.3(APOB):c.3096C>G (p.Thr1032=) rs757565957
NM_000384.3(APOB):c.3122-6G>A rs72653071
NM_000384.3(APOB):c.3337G>C (p.Asp1113His) rs12713844
NM_000384.3(APOB):c.3383G>A (p.Arg1128His) rs12713843
NM_000384.3(APOB):c.3426G>A (p.Ser1142=) rs142448733
NM_000384.3(APOB):c.3427C>T (p.Pro1143Ser) rs72653077
NM_000384.3(APOB):c.3509-10G>A rs12720770
NM_000384.3(APOB):c.3509-11C>T rs200768300
NM_000384.3(APOB):c.3595G>A (p.Asp1199Asn) rs375894411
NM_000384.3(APOB):c.3634C>A (p.Leu1212Met) rs61736761
NM_000384.3(APOB):c.3656C>T (p.Thr1219Ile) rs768005049
NM_000384.3(APOB):c.3851G>A (p.Arg1284Gln) rs372154910
NM_000384.3(APOB):c.4111G>A (p.Ala1371Thr) rs780170292
NM_000384.3(APOB):c.433C>T (p.Pro145Ser) rs6752026
NM_000384.3(APOB):c.4365C>T (p.Phe1455=) rs12720847
NM_000384.3(APOB):c.4532C>T (p.Thr1511Ile) rs146247063
NM_000384.3(APOB):c.4663A>G (p.Ile1555Val) rs141225768
NM_000384.3(APOB):c.4825T>C (p.Leu1609=) rs72653083
NM_000384.3(APOB):c.4929G>A (p.Ala1643=) rs200623857
NM_000384.3(APOB):c.5066G>A (p.Arg1689His) rs151009667
NM_000384.3(APOB):c.538-9C>T rs1800478
NM_000384.3(APOB):c.5560G>A (p.Asp1854Asn) rs138005301
NM_000384.3(APOB):c.5616C>T (p.Ile1872=) rs1487486971
NM_000384.3(APOB):c.5646C>G (p.Ser1882Arg) rs1012783946
NM_000384.3(APOB):c.5690G>A (p.Arg1897His) rs199510126
NM_000384.3(APOB):c.5715G>A (p.Met1905Ile) rs754036439
NM_000384.3(APOB):c.5741A>G (p.Asn1914Ser) rs1801699
NM_000384.3(APOB):c.581C>T (p.Thr194Met) rs13306198
NM_000384.3(APOB):c.5863G>A (p.Val1955Met) rs368970025
NM_000384.3(APOB):c.606A>T (p.Glu202Asp) rs61746672
NM_000384.3(APOB):c.607A>G (p.Ile203Val) rs72653059
NM_000384.3(APOB):c.6125T>C (p.Met2042Thr) rs371224295
NM_000384.3(APOB):c.6261C>A (p.Thr2087=) rs61744855
NM_000384.3(APOB):c.6636_6638TGA[1] (p.Asp2213del) rs541497967
NM_000384.3(APOB):c.6815A>G (p.His2272Arg) rs1553383649
NM_000384.3(APOB):c.6895G>C (p.Asp2299His) rs12713681
NM_000384.3(APOB):c.689G>T (p.Gly230Val) rs755661819
NM_000384.3(APOB):c.690C>A (p.Gly230=) rs151096846
NM_000384.3(APOB):c.6943G>A (p.Glu2315Lys) rs1223711938
NM_000384.3(APOB):c.7152T>C (p.Val2384=) rs72653090
NM_000384.3(APOB):c.7296C>T (p.Tyr2432=) rs1553383536
NM_000384.3(APOB):c.7330C>T (p.Arg2444Cys) rs754565622
NM_000384.3(APOB):c.7367C>A (p.Ala2456Asp) rs12713675
NM_000384.3(APOB):c.7612C>T (p.Leu2538=) rs72653093
NM_000384.3(APOB):c.7615G>A (p.Val2539Ile) rs148170480
NM_000384.3(APOB):c.7696G>A (p.Glu2566Lys) rs1801696
NM_000384.3(APOB):c.8148C>T (p.Ile2716=) rs6413458
NM_000384.3(APOB):c.830G>T (p.Gly277Val) rs1057516137
NM_000384.3(APOB):c.8353A>C (p.Asn2785His) rs2163204
NM_000384.3(APOB):c.8462C>T (p.Pro2821Leu) rs72653095
NM_000384.3(APOB):c.8469T>C (p.Ala2823=) rs531216195
NM_000384.3(APOB):c.8550T>G (p.Ile2850Met) rs148498577
NM_000384.3(APOB):c.8693T>C (p.Leu2898Pro) rs376974746
NM_000384.3(APOB):c.8877G>A (p.Leu2959=) rs765899256
NM_000384.3(APOB):c.889C>T (p.Arg297Cys) rs766376456
NM_000384.3(APOB):c.900T>C (p.Gly300=) rs549628916
NM_000384.3(APOB):c.905-15C>G rs72653061
NM_000384.3(APOB):c.9095C>A (p.Thr3032Asn) rs754332101
NM_000384.3(APOB):c.9105T>C (p.Asn3035=) rs147510760
NM_000384.3(APOB):c.9294C>T (p.Tyr3098=) rs145777339
NM_000384.3(APOB):c.9387T>G (p.Pro3129=) rs769437017
NM_000384.3(APOB):c.9471C>T (p.Gly3157=) rs746031928
NM_000384.3(APOB):c.9477G>A (p.Lys3159=) rs13306196
NM_000384.3(APOB):c.9633C>A (p.Asn3211Lys) rs748318755
NM_000384.3(APOB):c.9639C>A (p.Asn3213Lys) rs574725520
NM_000384.3(APOB):c.9694A>G (p.Lys3232Glu) rs544521341
NM_000384.3(APOB):c.9811G>A (p.Gly3271Ser) rs142422341
NM_000384.3(APOB):c.9835A>G (p.Ser3279Gly) rs12720854
NM_000384.3(APOB):c.9855C>T (p.Ile3285=) rs72654403
NM_000384.3(APOB):c.9880T>C (p.Ser3294Pro) rs12720855
NM_000384.3(APOB):c.9883T>C (p.Tyr3295His) rs186299244

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.