ClinVar Miner

List of variants in gene APOB studied for not provided

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Total variants: 70
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HGVS dbSNP
NM_000384.2(APOB):c.10131G>A (p.Leu3377=) rs1799812
NM_000384.2(APOB):c.10294C>G (p.Gln3432Glu) rs1042023
NM_000384.2(APOB):c.1033G>A (p.Ala345Thr)
NM_000384.2(APOB):c.10579C>T (p.Arg3527Trp) rs144467873
NM_000384.2(APOB):c.10580G>A (p.Arg3527Gln) rs5742904
NM_000384.2(APOB):c.10672C>T (p.Arg3558Cys) rs12713559
NM_000384.2(APOB):c.10701G>A (p.Thr3567=) rs12713558
NM_000384.2(APOB):c.10708C>T (p.His3570Tyr) rs201736972
NM_000384.2(APOB):c.10737C>T (p.Thr3579=) rs12713554
NM_000384.2(APOB):c.10740C>T (p.Asn3580=) rs150312765
NM_000384.2(APOB):c.10778C>T (p.Pro3593Leu) rs1553382921
NM_000384.2(APOB):c.10848delT (p.Gly3617Alafs) rs982371659
NM_000384.2(APOB):c.11257T>C (p.Phe3753Leu) rs61741974
NM_000384.2(APOB):c.11789-8C>T rs201274370
NM_000384.2(APOB):c.11808C>T (p.Ile3936=) rs12720852
NM_000384.2(APOB):c.11966G>A (p.Arg3989His) rs148197354
NM_000384.2(APOB):c.12148G>A (p.Glu4050Lys) rs201448956
NM_000384.2(APOB):c.1223T>C (p.Ile408Thr) rs12714225
NM_000384.2(APOB):c.12382G>A (p.Val4128Met) rs1801703
NM_000384.2(APOB):c.12697T>A (p.Ser4233Thr) rs61743299
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.13441G>A (p.Ala4481Thr) rs1801695
NM_000384.2(APOB):c.13566C>T (p.Asp4522=) rs371437581
NM_000384.2(APOB):c.1648G>C (p.Asp550His) rs145862664
NM_000384.2(APOB):c.1753C>A (p.Gln585Lys) rs140101603
NM_000384.2(APOB):c.2188G>A (p.Val730Ile) rs12691202
NM_000384.2(APOB):c.2222C>A (p.Thr741Asn) rs12714192
NM_000384.2(APOB):c.2302A>G (p.Lys768Glu) rs1553385712
NM_000384.2(APOB):c.2691T>G (p.Ser897Arg) rs144806800
NM_000384.2(APOB):c.288G>T (p.Gln96His) rs186544754
NM_000384.2(APOB):c.2981C>T (p.Pro994Leu) rs41288783
NM_000384.2(APOB):c.307T>C (p.Tyr103His) rs9282603
NM_000384.2(APOB):c.3383G>A (p.Arg1128His) rs12713843
NM_000384.2(APOB):c.3509-10G>A rs12720770
NM_000384.2(APOB):c.3634C>A (p.Leu1212Met) rs61736761
NM_000384.2(APOB):c.3709T>G (p.Trp1237Gly) rs935161396
NM_000384.2(APOB):c.3829C>T (p.Leu1277Phe) rs544542990
NM_000384.2(APOB):c.4187T>C (p.Val1396Ala) rs144034290
NM_000384.2(APOB):c.433C>T (p.Pro145Ser) rs6752026
NM_000384.2(APOB):c.4471A>T (p.Arg1491Ter)
NM_000384.2(APOB):c.4532C>T (p.Thr1511Ile) rs146247063
NM_000384.2(APOB):c.4796G>T (p.Arg1599Leu) rs746414462
NM_000384.2(APOB):c.5065C>T (p.Arg1689Cys) rs780820172
NM_000384.2(APOB):c.5201_5203delAAG (p.Glu1734del) rs1553383904
NM_000384.2(APOB):c.5459A>C (p.Lys1820Thr) rs180874451
NM_000384.2(APOB):c.5562C>A (p.Asp1854Glu) rs386352278
NM_000384.2(APOB):c.5741A>G (p.Asn1914Ser) rs1801699
NM_000384.2(APOB):c.5991T>A (p.Asp1997Glu) rs768045701
NM_000384.2(APOB):c.606A>T (p.Glu202Asp) rs61746672
NM_000384.2(APOB):c.6261C>A (p.Thr2087=) rs61744855
NM_000384.2(APOB):c.6659T>C (p.Val2220Ala) rs374736992
NM_000384.2(APOB):c.6874A>C (p.Ile2292Leu) rs1553383634
NM_000384.2(APOB):c.6961G>C (p.Val2321Leu) rs1085307523
NM_000384.2(APOB):c.7152T>C (p.Val2384=) rs72653090
NM_000384.2(APOB):c.7285T>A (p.Ser2429Thr) rs72653092
NM_000384.2(APOB):c.7367C>A (p.Ala2456Asp) rs12713675
NM_000384.2(APOB):c.7565G>A (p.Arg2522Gln) rs781243278
NM_000384.2(APOB):c.7696G>A (p.Glu2566Lys) rs1801696
NM_000384.2(APOB):c.7851delT (p.Phe2617Leufs) rs1220363895
NM_000384.2(APOB):c.8148C>T (p.Ile2716=) rs6413458
NM_000384.2(APOB):c.8661T>C (p.Thr2887=)
NM_000384.2(APOB):c.9004C>T (p.Leu3002=) rs12713600
NM_000384.2(APOB):c.9110T>G (p.Leu3037Arg)
NM_000384.2(APOB):c.9242G>C (p.Ser3081Thr) rs72653100
NM_000384.2(APOB):c.9407G>A (p.Arg3136His) rs199590149
NM_000384.2(APOB):c.9639C>A (p.Asn3213Lys) rs574725520
NM_000384.2(APOB):c.9880T>C (p.Ser3294Pro) rs12720855
NM_000384.3(APOB):c.11092A>G (p.Arg3698Gly)
NM_000384.3(APOB):c.2096C>T (p.Pro699Leu)

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