ClinVar Miner

List of variants in gene APOB reported as uncertain significance for not specified

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Total variants: 44
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HGVS dbSNP gnomAD frequency
NM_000384.3(APOB):c.7696G>A (p.Glu2566Lys) rs1801696 0.00305
NM_000384.3(APOB):c.3740A>G (p.Tyr1247Cys) rs61741164 0.00071
NM_000384.3(APOB):c.925G>A (p.Ala309Thr) rs141888564 0.00026
NM_000384.3(APOB):c.9639C>A (p.Asn3213Lys) rs574725520 0.00025
NM_000384.3(APOB):c.5599C>T (p.Arg1867Trp) rs200583769 0.00024
NM_000384.3(APOB):c.8550T>G (p.Ile2850Met) rs148498577 0.00024
NM_000384.3(APOB):c.10708C>T (p.His3570Tyr) rs201736972 0.00021
NM_000384.3(APOB):c.13181T>C (p.Val4394Ala) rs12720843 0.00017
NM_000384.3(APOB):c.2914G>A (p.Gly972Ser) rs199893862 0.00014
NM_000384.3(APOB):c.10402A>G (p.Met3468Val) rs149887185 0.00009
NM_000384.3(APOB):c.10700C>T (p.Thr3567Met) rs368278927 0.00009
NM_000384.3(APOB):c.13175G>A (p.Ser4392Asn) rs777718986 0.00008
NM_000384.3(APOB):c.13288T>A (p.Ser4430Thr) rs72654426 0.00008
NM_000384.3(APOB):c.6655C>T (p.Arg2219Cys) rs141641980 0.00007
NM_000384.3(APOB):c.2536T>A (p.Leu846Met) rs189880634 0.00006
NM_000384.3(APOB):c.7698G>C (p.Glu2566Asp) rs149306841 0.00006
NM_000384.3(APOB):c.7330C>T (p.Arg2444Cys) rs754565622 0.00004
NM_000384.3(APOB):c.10541C>T (p.Ala3514Val) rs1450324476 0.00003
NM_000384.3(APOB):c.7853T>C (p.Ile2618Thr) rs531273434 0.00003
NM_000384.3(APOB):c.10535C>T (p.Thr3512Ile) rs145861016 0.00001
NM_000384.3(APOB):c.13154G>A (p.Arg4385His) rs533755016 0.00001
NM_000384.3(APOB):c.6389A>G (p.Asn2130Ser) rs1359479064 0.00001
NM_000384.3(APOB):c.10304T>A (p.Ile3435Asn)
NM_000384.3(APOB):c.10345A>G (p.Lys3449Glu) rs967810441
NM_000384.3(APOB):c.10403T>A (p.Met3468Lys) rs1572778607
NM_000384.3(APOB):c.10556C>T (p.Thr3519Ile) rs746951119
NM_000384.3(APOB):c.10672C>T (p.Arg3558Cys)
NM_000384.3(APOB):c.10753A>G (p.Ser3585Gly)
NM_000384.3(APOB):c.10874A>G (p.Asn3625Ser) rs1663126182
NM_000384.3(APOB):c.11683A>C (p.Asn3895His) rs2103350346
NM_000384.3(APOB):c.11761G>A (p.Val3921Ile)
NM_000384.3(APOB):c.13028_13029del (p.Tyr4343fs) rs760832994
NM_000384.3(APOB):c.13477CAG[1] (p.Gln4494del) rs562574661
NM_000384.3(APOB):c.2188G>A (p.Val730Ile)
NM_000384.3(APOB):c.2245G>T (p.Asp749Tyr) rs1663700975
NM_000384.3(APOB):c.2981C>T (p.Pro994Leu)
NM_000384.3(APOB):c.3427C>T (p.Pro1143Ser)
NM_000384.3(APOB):c.3491G>C (p.Arg1164Thr)
NM_000384.3(APOB):c.4246_4251del (p.Asn1416_Thr1417del) rs767878127
NM_000384.3(APOB):c.5066G>A (p.Arg1689His)
NM_000384.3(APOB):c.5689C>T (p.Arg1897Cys) rs189341276
NM_000384.3(APOB):c.6640G>A (p.Glu2214Lys) rs1239957664
NM_000384.3(APOB):c.7285T>A (p.Ser2429Thr)
NM_000384.3(APOB):c.9175C>T (p.Arg3059Cys)

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