ClinVar Miner

List of variants in gene APOB reported as uncertain significance by Robarts Research Institute, Western University

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Total variants: 51
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HGVS dbSNP gnomAD frequency
NM_000384.3(APOB):c.1353-12C>T rs76202659 0.01423
NM_000384.3(APOB):c.11833A>G (p.Thr3945Ala) rs1801698 0.00212
NM_000384.3(APOB):c.3509-11C>T rs200768300 0.00091
NM_000384.3(APOB):c.1470+15T>C rs185550846 0.00078
NM_000384.3(APOB):c.9883T>C (p.Tyr3295His) rs186299244 0.00027
NM_000384.3(APOB):c.9639C>A (p.Asn3213Lys) rs574725520 0.00025
NM_000384.3(APOB):c.8550T>G (p.Ile2850Met) rs148498577 0.00024
NM_000384.3(APOB):c.4532C>T (p.Thr1511Ile) rs146247063 0.00019
NM_000384.3(APOB):c.9811G>A (p.Gly3271Ser) rs142422341 0.00019
NM_000384.3(APOB):c.4111G>A (p.Ala1371Thr) rs780170292 0.00011
NM_000384.3(APOB):c.11965C>T (p.Arg3989Cys) rs150713761 0.00010
NM_000384.3(APOB):c.10508C>T (p.Ser3503Leu) rs375284245 0.00007
NM_000384.3(APOB):c.5560G>A (p.Asp1854Asn) rs138005301 0.00006
NM_000384.3(APOB):c.5863G>A (p.Val1955Met) rs368970025 0.00006
NM_000384.3(APOB):c.6125T>C (p.Met2042Thr) rs371224295 0.00005
NM_000384.3(APOB):c.1061A>G (p.Glu354Gly) rs149227065 0.00004
NM_000384.3(APOB):c.11509G>T (p.Ala3837Ser) rs1389480980 0.00004
NM_000384.3(APOB):c.3656C>T (p.Thr1219Ile) rs768005049 0.00004
NM_000384.3(APOB):c.7330C>T (p.Arg2444Cys) rs754565622 0.00004
NM_000384.3(APOB):c.9694A>G (p.Lys3232Glu) rs544521341 0.00004
NM_000384.3(APOB):c.3851G>A (p.Arg1284Gln) rs372154910 0.00003
NM_000384.3(APOB):c.8693T>C (p.Leu2898Pro) rs376974746 0.00003
NM_000384.3(APOB):c.889C>T (p.Arg297Cys) rs766376456 0.00003
NM_000384.3(APOB):c.5690G>A (p.Arg1897His) rs199510126 0.00002
NM_000384.3(APOB):c.9095C>A (p.Thr3032Asn) rs754332101 0.00002
NM_000384.3(APOB):c.11356C>T (p.Leu3786Phe) rs571485213 0.00001
NM_000384.3(APOB):c.1198C>T (p.Arg400Cys) rs778866803 0.00001
NM_000384.3(APOB):c.13160A>T (p.Glu4387Val) rs150412734 0.00001
NM_000384.3(APOB):c.1617+7T>C rs374552390 0.00001
NM_000384.3(APOB):c.5646C>G (p.Ser1882Arg) rs1012783946 0.00001
NM_000384.3(APOB):c.6943G>A (p.Glu2315Lys) rs1223711938 0.00001
NM_000384.3(APOB):c.9633C>A (p.Asn3211Lys) rs748318755 0.00001
NM_000384.3(APOB):c.10061C>G (p.Ala3354Gly)
NM_000384.3(APOB):c.10367C>T (p.Ser3456Phe) rs1217782046
NM_000384.3(APOB):c.10780T>C (p.Trp3594Arg)
NM_000384.3(APOB):c.11401T>A (p.Ser3801Thr)
NM_000384.3(APOB):c.11477C>T (p.Thr3826Met)
NM_000384.3(APOB):c.12310C>A (p.Leu4104Met) rs199668351
NM_000384.3(APOB):c.12343G>A (p.Val4115Ile) rs765681925
NM_000384.3(APOB):c.13477CAG[1] (p.Gln4494del) rs562574661
NM_000384.3(APOB):c.1618-13C>T rs1553386146
NM_000384.3(APOB):c.3122-6G>A rs72653071
NM_000384.3(APOB):c.3427C>T (p.Pro1143Ser)
NM_000384.3(APOB):c.3595G>A (p.Asp1199Asn) rs375894411
NM_000384.3(APOB):c.4663A>G (p.Ile1555Val)
NM_000384.3(APOB):c.5066G>A (p.Arg1689His)
NM_000384.3(APOB):c.5715G>A (p.Met1905Ile) rs754036439
NM_000384.3(APOB):c.6815A>G (p.His2272Arg) rs1553383649
NM_000384.3(APOB):c.689G>T (p.Gly230Val) rs755661819
NM_000384.3(APOB):c.7367C>A (p.Ala2456Asp)
NM_000384.3(APOB):c.830G>T (p.Gly277Val) rs1057516137

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