ClinVar Miner

List of variants in gene APOB reported as likely benign by Invitae

Minimum submission review status: Collection method:
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Gene type:
ClinVar version:
Total variants: 93
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HGVS dbSNP
NM_000384.3(APOB):c.10056C>A (p.Thr3352=) rs369022661
NM_000384.3(APOB):c.10371C>T (p.Ser3457=) rs139891446
NM_000384.3(APOB):c.1053G>T (p.Leu351=) rs772126283
NM_000384.3(APOB):c.10575C>T (p.Ser3525=) rs142573551
NM_000384.3(APOB):c.10701G>T (p.Thr3567=) rs12713558
NM_000384.3(APOB):c.11091T>C (p.Gly3697=) rs201368496
NM_000384.3(APOB):c.11354C>T (p.Thr3785Ile) rs143710616
NM_000384.3(APOB):c.11401T>A (p.Ser3801Thr) rs12713540
NM_000384.3(APOB):c.11442C>T (p.Thr3814=) rs72654408
NM_000384.3(APOB):c.11676C>T (p.Pro3892=) rs762760699
NM_000384.3(APOB):c.11720A>G (p.Asp3907Gly) rs61746686
NM_000384.3(APOB):c.11733A>T (p.Thr3911=) rs1553382722
NM_000384.3(APOB):c.11782C>T (p.Leu3928=) rs764635907
NM_000384.3(APOB):c.11820G>A (p.Thr3940=) rs72654417
NM_000384.3(APOB):c.11934C>T (p.Ile3978=) rs539824713
NM_000384.3(APOB):c.1199G>A (p.Arg400His) rs530171166
NM_000384.3(APOB):c.12021C>A (p.Gly4007=) rs145498491
NM_000384.3(APOB):c.12088-10C>T rs1193057149
NM_000384.3(APOB):c.12444C>A (p.Ala4148=) rs757789853
NM_000384.3(APOB):c.12903C>T (p.Asp4301=) rs200145506
NM_000384.3(APOB):c.1298C>T (p.Ala433Val) rs13306190
NM_000384.3(APOB):c.13102C>G (p.Gln4368Glu) rs72654424
NM_000384.3(APOB):c.1310G>A (p.Arg437His) rs142114415
NM_000384.3(APOB):c.13452G>A (p.Thr4484=) rs200374122
NM_000384.3(APOB):c.1410G>C (p.Leu470=) rs368305590
NM_000384.3(APOB):c.1470+8C>T rs779326198
NM_000384.3(APOB):c.1605G>A (p.Glu535=) rs763856498
NM_000384.3(APOB):c.1648G>C (p.Asp550His) rs145862664
NM_000384.3(APOB):c.1741C>T (p.Leu581=) rs775852055
NM_000384.3(APOB):c.244C>T (p.Leu82=) rs201658954
NM_000384.3(APOB):c.2550A>C (p.Ser850=) rs146519598
NM_000384.3(APOB):c.2568C>T (p.Pro856=) rs184556149
NM_000384.3(APOB):c.2630C>T (p.Pro877Leu) rs12714097
NM_000384.3(APOB):c.2655A>G (p.Thr885=) rs368844493
NM_000384.3(APOB):c.2841C>T (p.Thr947=) rs72653070
NM_000384.3(APOB):c.2853G>A (p.Glu951=) rs151193347
NM_000384.3(APOB):c.285C>A (p.Ser95Arg) rs143613534
NM_000384.3(APOB):c.2863C>T (p.Pro955Ser) rs13306206
NM_000384.3(APOB):c.2949C>T (p.Asn983=) rs760094793
NM_000384.3(APOB):c.2981C>T (p.Pro994Leu) rs41288783
NM_000384.3(APOB):c.2988C>T (p.Thr996=) rs137875230
NM_000384.3(APOB):c.2994C>T (p.Asp998=) rs777501128
NM_000384.3(APOB):c.307T>C (p.Tyr103His) rs9282603
NM_000384.3(APOB):c.3081A>G (p.Arg1027=) rs750932563
NM_000384.3(APOB):c.3122-6G>T rs72653071
NM_000384.3(APOB):c.3256G>A (p.Gly1086Ser) rs12720801
NM_000384.3(APOB):c.3427C>T (p.Pro1143Ser) rs72653077
NM_000384.3(APOB):c.3712C>A (p.Leu1238Ile) rs72653078
NM_000384.3(APOB):c.3740A>G (p.Tyr1247Cys) rs61741164
NM_000384.3(APOB):c.3971A>C (p.Lys1324Thr) rs763846768
NM_000384.3(APOB):c.4178C>T (p.Ala1393Val) rs143282164
NM_000384.3(APOB):c.420G>A (p.Gln140=) rs758439614
NM_000384.3(APOB):c.4590C>T (p.Thr1530=) rs1420371568
NM_000384.3(APOB):c.4656T>C (p.Ser1552=) rs761580028
NM_000384.3(APOB):c.465C>T (p.Asn155=) rs1195121842
NM_000384.3(APOB):c.4796G>A (p.Arg1599His) rs746414462
NM_000384.3(APOB):c.4838G>C (p.Ser1613Thr) rs61742247
NM_000384.3(APOB):c.5066G>A (p.Arg1689His) rs151009667
NM_000384.3(APOB):c.5145G>A (p.Gln1715=) rs1553383921
NM_000384.3(APOB):c.5183A>G (p.Asn1728Ser) rs186346145
NM_000384.3(APOB):c.5706G>A (p.Pro1902=) rs145277222
NM_000384.3(APOB):c.5763A>G (p.Gly1921=) rs141022509
NM_000384.3(APOB):c.5913G>A (p.Leu1971=) rs374251542
NM_000384.3(APOB):c.6021G>C (p.Val2007=) rs148252000
NM_000384.3(APOB):c.6283G>A (p.Val2095Ile) rs200874264
NM_000384.3(APOB):c.6390T>C (p.Asn2130=) rs570798466
NM_000384.3(APOB):c.641G>A (p.Arg214His) rs146152405
NM_000384.3(APOB):c.6656G>A (p.Arg2219His) rs200106845
NM_000384.3(APOB):c.690C>A (p.Gly230=) rs151096846
NM_000384.3(APOB):c.6972T>C (p.Leu2324=) rs1553383600
NM_000384.3(APOB):c.7011C>T (p.Phe2337=) rs776099551
NM_000384.3(APOB):c.7128G>A (p.Lys2376=) rs368448196
NM_000384.3(APOB):c.7152T>C (p.Val2384=) rs72653090
NM_000384.3(APOB):c.7223C>T (p.Ser2408Phe) rs140027955
NM_000384.3(APOB):c.7285T>A (p.Ser2429Thr) rs72653092
NM_000384.3(APOB):c.7587G>A (p.Gln2529=) rs752939907
NM_000384.3(APOB):c.7683T>C (p.Leu2561=) rs781283777
NM_000384.3(APOB):c.7794T>G (p.Pro2598=) rs1553383444
NM_000384.3(APOB):c.7863A>C (p.Leu2621=) rs138497378
NM_000384.3(APOB):c.7989T>C (p.Ile2663=) rs199642915
NM_000384.3(APOB):c.7998A>G (p.Val2666=) rs1042006
NM_000384.3(APOB):c.8309C>T (p.Thr2770Ile) rs138391809
NM_000384.3(APOB):c.8766T>G (p.Thr2922=) rs763285729
NM_000384.3(APOB):c.8912A>C (p.Asn2971Thr) rs72653098
NM_000384.3(APOB):c.895T>G (p.Phe299Val) rs72653060
NM_000384.3(APOB):c.9226C>A (p.Leu3076Met) rs72653099
NM_000384.3(APOB):c.9354T>C (p.Asn3118=) rs1553383179
NM_000384.3(APOB):c.9639C>A (p.Asn3213Lys) rs574725520
NM_000384.3(APOB):c.9810C>T (p.Phe3270=) rs138010392
NM_000384.3(APOB):c.9883T>C (p.Tyr3295His) rs186299244
NM_000384.3(APOB):c.9930T>C (p.Pro3310=) rs764448582
NM_000384.3(APOB):c.9937C>A (p.Leu3313Ile) rs146687604
NM_000384.3(APOB):c.9975C>A (p.Thr3325=) rs1226284347

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