ClinVar Miner

List of variants in gene APOB reported by CeGaT Center for Human Genetics Tuebingen

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Gene type:
ClinVar version:
Total variants: 100
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HGVS dbSNP gnomAD frequency
NM_000384.3(APOB):c.8148C>T (p.Ile2716=) rs6413458 0.02288
NM_000384.3(APOB):c.10131G>A (p.Leu3377=) rs1799812 0.00564
NM_000384.3(APOB):c.905-15C>G rs72653061 0.00554
NM_000384.3(APOB):c.12794T>C (p.Val4265Ala) rs61743502 0.00516
NM_000384.3(APOB):c.606A>T (p.Glu202Asp) rs61746672 0.00387
NM_000384.3(APOB):c.6261C>A (p.Thr2087=) rs61744855 0.00366
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.4825T>C (p.Leu1609=) rs72653083 0.00242
NM_000384.3(APOB):c.7615G>A (p.Val2539Ile) rs148170480 0.00210
NM_000384.3(APOB):c.751G>A (p.Ala251Thr) rs61741625 0.00190
NM_000384.3(APOB):c.3426G>A (p.Ser1142=) rs142448733 0.00177
NM_000384.3(APOB):c.9105T>C (p.Asn3035=) rs147510760 0.00166
NM_000384.3(APOB):c.9294C>T (p.Tyr3098=) rs145777339 0.00139
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.12807T>C (p.Tyr4269=) rs181340304 0.00093
NM_000384.3(APOB):c.4838G>C (p.Ser1613Thr) rs61742247 0.00093
NM_000384.3(APOB):c.3178T>C (p.Leu1060=) rs72653073 0.00078
NM_000384.3(APOB):c.4178C>T (p.Ala1393Val) rs143282164 0.00073
NM_000384.3(APOB):c.2630C>T (p.Pro877Leu) rs12714097 0.00063
NM_000384.3(APOB):c.9855C>T (p.Ile3285=) rs72654403 0.00041
NM_000384.3(APOB):c.3382C>T (p.Arg1128Cys) rs72653076 0.00039
NM_000384.3(APOB):c.2853G>A (p.Glu951=) rs151193347 0.00031
NM_000384.3(APOB):c.914A>G (p.Lys305Arg) rs199937544 0.00029
NM_000384.3(APOB):c.8912A>C (p.Asn2971Thr) rs72653098 0.00026
NM_000384.3(APOB):c.925G>A (p.Ala309Thr) rs141888564 0.00026
NM_000384.3(APOB):c.8550T>G (p.Ile2850Met) rs148498577 0.00024
NM_000384.3(APOB):c.7863A>C (p.Leu2621=) rs138497378 0.00022
NM_000384.3(APOB):c.13020T>C (p.Tyr4340=) rs141339310 0.00021
NM_000384.3(APOB):c.4449A>G (p.Glu1483=) rs151018874 0.00020
NM_000384.3(APOB):c.11354C>T (p.Thr3785Ile) rs143710616 0.00019
NM_000384.3(APOB):c.11442C>T (p.Thr3814=) rs72654408 0.00016
NM_000384.3(APOB):c.244C>T (p.Leu82=) rs201658954 0.00014
NM_000384.3(APOB):c.13302C>T (p.Ser4434=) rs144040999 0.00013
NM_000384.3(APOB):c.3049A>C (p.Ser1017Arg) rs149323475 0.00013
NM_000384.3(APOB):c.6655C>T (p.Arg2219Cys) rs141641980 0.00007
NM_000384.3(APOB):c.7998A>G (p.Val2666=) rs1042006 0.00007
NM_000384.3(APOB):c.8134C>T (p.Arg2712Cys) rs372245645 0.00006
NM_000384.3(APOB):c.12381C>T (p.Asp4127=) rs145704672 0.00005
NM_000384.3(APOB):c.13452G>A (p.Thr4484=) rs200374122 0.00005
NM_000384.3(APOB):c.5913G>A (p.Leu1971=) rs374251542 0.00005
NM_000384.3(APOB):c.1992T>G (p.Asn664Lys) rs777320899 0.00004
NM_000384.3(APOB):c.4257A>G (p.Thr1419=) rs778729560 0.00004
NM_000384.3(APOB):c.573C>T (p.Thr191=) rs202005055 0.00004
NM_000384.3(APOB):c.6201C>T (p.His2067=) rs143222685 0.00004
NM_000384.3(APOB):c.6875T>C (p.Ile2292Thr) rs145977507 0.00004
NM_000384.3(APOB):c.6927A>G (p.Arg2309=) rs201066460 0.00004
NM_000384.3(APOB):c.10416C>T (p.Thr3472=) rs558589282 0.00003
NM_000384.3(APOB):c.1518C>G (p.Leu506=) rs145849843 0.00003
NM_000384.3(APOB):c.3774G>C (p.Leu1258=) rs752823240 0.00003
NM_000384.3(APOB):c.11361C>T (p.Pro3787=) rs200979977 0.00002
NM_000384.3(APOB):c.435G>A (p.Pro145=) rs576323709 0.00002
NM_000384.3(APOB):c.6070A>G (p.Ile2024Val) rs564588440 0.00002
NM_000384.3(APOB):c.8052G>A (p.Leu2684=) rs778351930 0.00002
NM_000384.3(APOB):c.8367C>T (p.Ile2789=) rs149734450 0.00002
NM_000384.3(APOB):c.11033C>T (p.Pro3678Leu) rs1278748798 0.00001
NM_000384.3(APOB):c.12343G>T (p.Val4115Phe) rs765681925 0.00001
NM_000384.3(APOB):c.12510C>T (p.Asn4170=) rs764649432 0.00001
NM_000384.3(APOB):c.3404G>A (p.Ser1135Asn) rs778519921 0.00001
NM_000384.3(APOB):c.4258C>T (p.Leu1420=) rs1483573722 0.00001
NM_000384.3(APOB):c.6253C>T (p.Arg2085Ter) rs121918386 0.00001
NM_000384.3(APOB):c.9717C>T (p.His3239=) rs150668826 0.00001
NM_000384.3(APOB):c.10294C>G (p.Gln3432Glu)
NM_000384.3(APOB):c.10580G>A (p.Arg3527Gln)
NM_000384.3(APOB):c.10932C>A (p.Phe3644Leu) rs1572777987
NM_000384.3(APOB):c.11124del (p.Phe3708fs) rs1282116285
NM_000384.3(APOB):c.11401T>A (p.Ser3801Thr)
NM_000384.3(APOB):c.11461A>G (p.Thr3821Ala) rs777808452
NM_000384.3(APOB):c.11477C>T (p.Thr3826Met)
NM_000384.3(APOB):c.12382G>A (p.Val4128Met)
NM_000384.3(APOB):c.12940A>G (p.Ile4314Val)
NM_000384.3(APOB):c.13131C>A (p.Ile4377=) rs763250972
NM_000384.3(APOB):c.2148C>T (p.Asn716=) rs754169002
NM_000384.3(APOB):c.2478T>C (p.Phe826=) rs377697247
NM_000384.3(APOB):c.2786dup (p.Arg931fs) rs1553385404
NM_000384.3(APOB):c.2981C>T (p.Pro994Leu)
NM_000384.3(APOB):c.3122-6G>A rs72653071
NM_000384.3(APOB):c.3285C>T (p.Asp1095=)
NM_000384.3(APOB):c.3337G>C (p.Asp1113His)
NM_000384.3(APOB):c.3427C>T (p.Pro1143Ser)
NM_000384.3(APOB):c.4266T>C (p.Cys1422=)
NM_000384.3(APOB):c.4832del (p.Phe1611fs)
NM_000384.3(APOB):c.5066G>A (p.Arg1689His)
NM_000384.3(APOB):c.5163C>T (p.Val1721=) rs536182427
NM_000384.3(APOB):c.6636TGA[1] (p.Asp2213del) rs541497967
NM_000384.3(APOB):c.6679del (p.His2227fs) rs2103356720
NM_000384.3(APOB):c.6765G>A (p.Lys2255=) rs372343882
NM_000384.3(APOB):c.6874A>C (p.Ile2292Leu) rs1553383634
NM_000384.3(APOB):c.6895G>C (p.Asp2299His)
NM_000384.3(APOB):c.726C>T (p.Ser242=)
NM_000384.3(APOB):c.7285T>A (p.Ser2429Thr)
NM_000384.3(APOB):c.7520A>G (p.His2507Arg) rs766283781
NM_000384.3(APOB):c.7529C>T (p.Ala2510Val) rs1329248076
NM_000384.3(APOB):c.7619G>T (p.Gly2540Val) rs571626569
NM_000384.3(APOB):c.9140C>G (p.Thr3047Arg) rs61742323
NM_000384.3(APOB):c.9835A>G (p.Ser3279Gly)
NM_000384.3(APOB):c.9924T>C (p.His3308=) rs370661042

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