ClinVar Miner

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

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Gene type:
ClinVar version:
Total variants: 64
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HGVS dbSNP gnomAD frequency
NM_000384.3(APOB):c.433C>T (p.Pro145Ser) rs6752026 0.03579
NM_000384.3(APOB):c.13451C>T (p.Thr4484Met) rs12713450 0.03392
NM_000384.3(APOB):c.10737C>T (p.Thr3579=) rs12713554 0.02731
NM_000384.3(APOB):c.2222C>A (p.Thr741Asn) rs12714192 0.02253
NM_000384.3(APOB):c.10701G>A (p.Thr3567=) rs12713558 0.02176
NM_000384.3(APOB):c.4365C>T (p.Phe1455=) rs12720847 0.01812
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.9880T>C (p.Ser3294Pro) rs12720855 0.01525
NM_000384.3(APOB):c.12697T>A (p.Ser4233Thr) rs61743299 0.01522
NM_000384.3(APOB):c.9835A>G (p.Ser3279Gly) rs12720854 0.00761
NM_000384.3(APOB):c.3337G>C (p.Asp1113His) rs12713844 0.00735
NM_000384.3(APOB):c.6895G>C (p.Asp2299His) rs12713681 0.00709
NM_000384.3(APOB):c.1594C>T (p.Arg532Trp) rs13306194 0.00578
NM_000384.3(APOB):c.12382G>A (p.Val4128Met) rs1801703 0.00562
NM_000384.3(APOB):c.10131G>A (p.Leu3377=) rs1799812 0.00560
NM_000384.3(APOB):c.12940A>G (p.Ile4314Val) rs72654423 0.00557
NM_000384.3(APOB):c.607A>G (p.Ile203Val) rs72653059 0.00396
NM_000384.3(APOB):c.606A>T (p.Glu202Asp) rs61746672 0.00387
NM_000384.3(APOB):c.3383G>A (p.Arg1128His) rs12713843 0.00376
NM_000384.3(APOB):c.6261C>A (p.Thr2087=) rs61744855 0.00366
NM_000384.3(APOB):c.8462C>T (p.Pro2821Leu) rs72653095 0.00267
NM_000384.3(APOB):c.7696G>A (p.Glu2566Lys) rs1801696 0.00249
NM_000384.3(APOB):c.1785C>G (p.Ser595=) rs139864087 0.00247
NM_000384.3(APOB):c.4825T>C (p.Leu1609=) rs72653083 0.00242
NM_000384.3(APOB):c.581C>T (p.Thr194Met) rs13306198 0.00229
NM_000384.3(APOB):c.7615G>A (p.Val2539Ile) rs148170480 0.00210
NM_000384.3(APOB):c.3426G>A (p.Ser1142=) rs142448733 0.00180
NM_000384.3(APOB):c.9294C>T (p.Tyr3098=) rs145777339 0.00136
NM_000384.3(APOB):c.2068-4T>A rs41291161 0.00108
NM_000384.3(APOB):c.7612C>T (p.Leu2538=) rs72653093 0.00102
NM_000384.3(APOB):c.8469T>C (p.Ala2823=) rs531216195 0.00080
NM_000384.3(APOB):c.9477G>A (p.Lys3159=) rs13306196 0.00073
NM_000384.3(APOB):c.2630C>T (p.Pro877Leu) rs12714097 0.00063
NM_000384.3(APOB):c.2981C>T (p.Pro994Leu) rs41288783 0.00058
NM_000384.3(APOB):c.7152T>C (p.Val2384=) rs72653090 0.00042
NM_000384.3(APOB):c.9855C>T (p.Ile3285=) rs72654403 0.00041
NM_000384.3(APOB):c.12252T>C (p.Tyr4084=) rs138157751 0.00034
NM_000384.3(APOB):c.13302C>T (p.Ser4434=) rs144040999 0.00013
NM_000384.3(APOB):c.8877G>A (p.Leu2959=) rs765899256 0.00012
NM_000384.3(APOB):c.12318A>G (p.Arg4106=) rs375795401 0.00008
NM_000384.3(APOB):c.4929G>A (p.Ala1643=) rs200623857 0.00008
NM_000384.3(APOB):c.10371C>T (p.Ser3457=) rs139891446 0.00005
NM_000384.3(APOB):c.13452G>A (p.Thr4484=) rs200374122 0.00005
NM_000384.3(APOB):c.2950G>A (p.Ala984Thr) rs752149683 0.00005
NM_000384.3(APOB):c.900T>C (p.Gly300=) rs549628916 0.00005
NM_000384.3(APOB):c.2968G>A (p.Ala990Thr) rs139434026 0.00003
NM_000384.3(APOB):c.3096C>G (p.Thr1032=) rs757565957 0.00003
NM_000384.3(APOB):c.690C>A (p.Gly230=) rs151096846 0.00002
NM_000384.3(APOB):c.11934C>T (p.Ile3978=) rs539824713 0.00001
NM_000384.3(APOB):c.3051C>T (p.Ser1017=) rs558838327 0.00001
NM_000384.3(APOB):c.3052G>A (p.Ala1018Thr) rs149357946 0.00001
NM_000384.3(APOB):c.5616C>T (p.Ile1872=) rs1487486971 0.00001
NM_000384.3(APOB):c.10740C>T (p.Asn3580=) rs150312765
NM_000384.3(APOB):c.13116A>G (p.Gln4372=) rs755500550
NM_000384.3(APOB):c.1402A>G (p.Asn468Asp) rs886804701
NM_000384.3(APOB):c.1493C>T (p.Thr498Ile) rs758928147
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.2308G>A (p.Val770Ile) rs1415675587
NM_000384.3(APOB):c.6636TGA[1] (p.Asp2213del) rs541497967
NM_000384.3(APOB):c.7296C>T (p.Tyr2432=) rs1553383536
NM_000384.3(APOB):c.9387T>G (p.Pro3129=) rs769437017
NM_000384.3(APOB):c.9471C>T (p.Gly3157=) rs746031928

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