ClinVar Miner

List of variants in gene APOB reported as likely benign for not specified

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Gene type:
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Total variants: 67
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HGVS dbSNP
NM_000384.2(APOB):c.10371C>T (p.Ser3457=) rs139891446
NM_000384.2(APOB):c.10913G>A (p.Arg3638Gln) rs1801701
NM_000384.2(APOB):c.11244G>A (p.Thr3748=) rs72654406
NM_000384.2(APOB):c.11401T>A (p.Ser3801Thr) rs12713540
NM_000384.2(APOB):c.11442C>G (p.Thr3814=) rs72654408
NM_000384.2(APOB):c.11477C>T (p.Thr3826Met) rs61744153
NM_000384.2(APOB):c.11819C>T (p.Thr3940Met) rs72654416
NM_000384.2(APOB):c.11820G>A (p.Thr3940=) rs72654417
NM_000384.2(APOB):c.11833A>G (p.Thr3945Ala) rs1801698
NM_000384.2(APOB):c.12016G>A (p.Val4006Ile) rs183117027
NM_000384.2(APOB):c.12024C>T (p.Thr4008=) rs145269223
NM_000384.2(APOB):c.12088-14T>C rs182329513
NM_000384.2(APOB):c.1223T>C (p.Ile408Thr) rs12714225
NM_000384.2(APOB):c.12541G>A (p.Glu4181Lys) rs1042031
NM_000384.2(APOB):c.12636T>C (p.Thr4212=) rs772812955
NM_000384.2(APOB):c.12794T>C (p.Val4265Ala) rs61743502
NM_000384.2(APOB):c.12940A>G (p.Ile4314Val) rs72654423
NM_000384.2(APOB):c.13013G>A (p.Ser4338Asn) rs1042034
NM_000384.2(APOB):c.13154G>A (p.Arg4385His) rs533755016
NM_000384.2(APOB):c.13368C>A (p.Thr4456=) rs1553382258
NM_000384.2(APOB):c.13441G>A (p.Ala4481Thr) rs1801695
NM_000384.2(APOB):c.1353-12C>T rs76202659
NM_000384.2(APOB):c.1395C>T (p.Asp465=) rs757609661
NM_000384.2(APOB):c.1470+15T>C rs185550846
NM_000384.2(APOB):c.1594C>T (p.Arg532Trp) rs13306194
NM_000384.2(APOB):c.1853C>T (p.Ala618Val) rs679899
NM_000384.2(APOB):c.1903C>A (p.Arg635=) rs548108916
NM_000384.2(APOB):c.2068-4T>A rs41291161
NM_000384.2(APOB):c.2310C>T (p.Val770=) rs72653064
NM_000384.2(APOB):c.2437-17C>T rs764415047
NM_000384.2(APOB):c.2817-19T>G rs72653069
NM_000384.2(APOB):c.293C>T (p.Thr98Ile) rs1367117
NM_000384.2(APOB):c.3122-6G>A rs72653071
NM_000384.2(APOB):c.3178T>C (p.Leu1060=) rs72653073
NM_000384.2(APOB):c.3337G>C (p.Asp1113His) rs12713844
NM_000384.2(APOB):c.3383G>A (p.Arg1128His) rs12713843
NM_000384.2(APOB):c.3426G>A (p.Ser1142=) rs142448733
NM_000384.2(APOB):c.3507T>C (p.Tyr1169=) rs141763789
NM_000384.2(APOB):c.3508+17_3508+18delCT rs1553384473
NM_000384.2(APOB):c.3509-11C>T rs200768300
NM_000384.2(APOB):c.400G>T (p.Ala134Ser) rs368321279
NM_000384.2(APOB):c.4838G>C (p.Ser1613Thr) rs61742247
NM_000384.2(APOB):c.5741A>G (p.Asn1914Ser) rs1801699
NM_000384.2(APOB):c.6261C>A (p.Thr2087=) rs61744855
NM_000384.2(APOB):c.6639_6641delTGA (p.Asp2213del) rs541497967
NM_000384.2(APOB):c.6895G>C (p.Asp2299His) rs12713681
NM_000384.2(APOB):c.6936C>T (p.Asp2312=) rs1041968
NM_000384.2(APOB):c.7152T>C (p.Val2384=) rs72653090
NM_000384.2(APOB):c.751G>A (p.Ala251Thr) rs61741625
NM_000384.2(APOB):c.7545C>T (p.Thr2515=) rs693
NM_000384.2(APOB):c.7575A>G (p.Gln2525=) rs377302171
NM_000384.2(APOB):c.7612C>T (p.Leu2538=) rs72653093
NM_000384.2(APOB):c.7615G>A (p.Val2539Ile) rs148170480
NM_000384.2(APOB):c.7696G>A (p.Glu2566Lys) rs1801696
NM_000384.2(APOB):c.7930A>C (p.Arg2644=) rs1553383425
NM_000384.2(APOB):c.7998A>G (p.Val2666=) rs1042006
NM_000384.2(APOB):c.8216C>T (p.Pro2739Leu) rs676210
NM_000384.2(APOB):c.8462C>T (p.Pro2821Leu) rs72653095
NM_000384.2(APOB):c.8530C>T (p.Leu2844=) rs1553383318
NM_000384.2(APOB):c.8994C>T (p.Gly2998=) rs139332237
NM_000384.2(APOB):c.905-15C>G rs72653061
NM_000384.2(APOB):c.905-16A>C rs12720810
NM_000384.2(APOB):c.9105T>C (p.Asn3035=) rs147510760
NM_000384.2(APOB):c.9378A>G (p.Leu3126=) rs760776177
NM_000384.2(APOB):c.9477G>A (p.Lys3159=) rs13306196
NM_000384.2(APOB):c.9835A>G (p.Ser3279Gly) rs12720854
NM_000384.2(APOB):c.9855C>T (p.Ile3285=) rs72654403

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