ClinVar Miner

List of variants in gene APOB reported as likely benign by Molecular Diagnostic Laboratory for Inherited Cardiovascular Disease, Montreal Heart Institute

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Gene type:
ClinVar version:
Total variants: 79
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HGVS dbSNP gnomAD frequency
NM_000384.3(APOB):c.2222C>A (p.Thr741Asn) rs12714192 0.02253
NM_000384.3(APOB):c.5741A>G (p.Asn1914Ser) rs1801699 0.01706
NM_000384.3(APOB):c.9880T>C (p.Ser3294Pro) rs12720855 0.01525
NM_000384.3(APOB):c.7367C>A (p.Ala2456Asp) rs12713675 0.01524
NM_000384.3(APOB):c.12697T>A (p.Ser4233Thr) rs61743299 0.01522
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.10294C>G (p.Gln3432Glu) rs1042023 0.00669
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.12940A>G (p.Ile4314Val) rs72654423 0.00557
NM_000384.3(APOB):c.12794T>C (p.Val4265Ala) rs61743502 0.00516
NM_000384.3(APOB):c.8353A>C (p.Asn2785His) rs2163204 0.00400
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.8462C>T (p.Pro2821Leu) rs72653095 0.00267
NM_000384.3(APOB):c.10061C>G (p.Ala3354Gly) rs61742331 0.00256
NM_000384.3(APOB):c.581C>T (p.Thr194Met) rs13306198 0.00229
NM_000384.3(APOB):c.11833A>G (p.Thr3945Ala) rs1801698 0.00212
NM_000384.3(APOB):c.7242A>C (p.Glu2414Asp) rs72653091 0.00212
NM_000384.3(APOB):c.7615G>A (p.Val2539Ile) rs148170480 0.00210
NM_000384.3(APOB):c.3427C>T (p.Pro1143Ser) rs72653077 0.00198
NM_000384.3(APOB):c.9105T>C (p.Asn3035=) rs147510760 0.00166
NM_000384.3(APOB):c.5066G>A (p.Arg1689His) rs151009667 0.00137
NM_000384.3(APOB):c.11401T>A (p.Ser3801Thr) rs12713540 0.00127
NM_000384.3(APOB):c.2068-4T>A rs41291161 0.00108
NM_000384.3(APOB):c.4163G>A (p.Arg1388His) rs13306187 0.00106
NM_000384.3(APOB):c.7612C>T (p.Leu2538=) rs72653093 0.00102
NM_000384.3(APOB):c.3740A>G (p.Tyr1247Cys) rs61741164 0.00067
NM_000384.3(APOB):c.7285T>A (p.Ser2429Thr) rs72653092 0.00061
NM_000384.3(APOB):c.4663A>G (p.Ile1555Val) rs141225768 0.00059
NM_000384.3(APOB):c.2436+102A>G rs576999094 0.00042
NM_000384.3(APOB):c.9855C>T (p.Ile3285=) rs72654403 0.00041
NM_000384.3(APOB):c.2310C>T (p.Val770=) rs72653064 0.00035
NM_000384.3(APOB):c.12252T>C (p.Tyr4084=) rs138157751 0.00034
NM_000384.3(APOB):c.2853G>A (p.Glu951=) rs151193347 0.00034
NM_000384.3(APOB):c.9810C>T (p.Phe3270=) rs138010392 0.00027
NM_000384.3(APOB):c.8912A>C (p.Asn2971Thr) rs72653098 0.00026
NM_000384.3(APOB):c.5763A>G (p.Gly1921=) rs141022509 0.00023
NM_000384.3(APOB):c.12016G>A (p.Val4006Ile) rs183117027 0.00022
NM_000384.3(APOB):c.3507T>C (p.Tyr1169=) rs141763789 0.00021
NM_000384.3(APOB):c.13444A>G (p.Ile4482Val) rs142702699 0.00019
NM_000384.3(APOB):c.4371A>G (p.Ala1457=) rs201206305 0.00013
NM_000384.3(APOB):c.1343C>T (p.Ala448Val) rs148167725 0.00012
NM_000384.3(APOB):c.11542G>A (p.Ala3848Thr) rs61743512 0.00011
NM_000384.3(APOB):c.13288T>A (p.Ser4430Thr) rs72654426 0.00008
NM_000384.3(APOB):c.2841C>T (p.Thr947=) rs72653070 0.00008
NM_000384.3(APOB):c.12736T>G (p.Phe4246Val) rs200260789 0.00007
NM_000384.3(APOB):c.7998A>G (p.Val2666=) rs1042006 0.00007
NM_000384.3(APOB):c.11319G>A (p.Lys3773=) rs780811733 0.00004
NM_000384.3(APOB):c.6125T>C (p.Met2042Thr) rs371224295 0.00004
NM_000384.3(APOB):c.3125C>T (p.Ala1042Val) rs61741467 0.00003
NM_000384.3(APOB):c.4181A>G (p.Asp1394Gly) rs769694008 0.00003
NM_000384.3(APOB):c.4590C>T (p.Thr1530=) rs1420371568 0.00003
NM_000384.3(APOB):c.13377T>C (p.Asp4459=) rs746353350 0.00002
NM_000384.3(APOB):c.690C>A (p.Gly230=) rs151096846 0.00002
NM_000384.3(APOB):c.11361C>T (p.Pro3787=) rs200979977 0.00001
NM_000384.3(APOB):c.12087+9C>T rs1298785033 0.00001
NM_000384.3(APOB):c.1251G>C (p.Leu417=) rs1248243388 0.00001
NM_000384.3(APOB):c.13488A>G (p.Arg4496=) rs755251454 0.00001
NM_000384.3(APOB):c.1617+7T>C rs374552390 0.00001
NM_000384.3(APOB):c.339G>C (p.Leu113=) rs1367232226 0.00001
NM_000384.3(APOB):c.3692T>C (p.Ile1231Thr) rs1663429897 0.00001
NM_000384.3(APOB):c.384-8_384-5del rs1206070366 0.00001
NM_000384.3(APOB):c.4818C>T (p.Tyr1606=) rs564437453 0.00001
NM_000384.3(APOB):c.8724C>T (p.Asn2908=) rs755498745 0.00001
NM_000384.3(APOB):c.1071C>T (p.Gly357=) rs769527337
NM_000384.3(APOB):c.11477C>T (p.Thr3826Met) rs61744153
NM_000384.3(APOB):c.1310G>A (p.Arg437His) rs142114415
NM_000384.3(APOB):c.1661C>T (p.Pro554Leu) rs12714214
NM_000384.3(APOB):c.3122-6G>A rs72653071
NM_000384.3(APOB):c.4066C>T (p.Leu1356=)
NM_000384.3(APOB):c.4140A>G (p.Thr1380=) rs781016611
NM_000384.3(APOB):c.4162C>T (p.Arg1388Cys) rs267599185
NM_000384.3(APOB):c.6636TGA[1] (p.Asp2213del) rs541497967
NM_000384.3(APOB):c.7930A>C (p.Arg2644=) rs1553383425
NM_000384.3(APOB):c.9242G>C (p.Ser3081Thr) rs72653100
NM_000384.3(APOB):c.9471C>T (p.Gly3157=) rs746031928

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