ClinVar Miner

List of variants in gene APOB reported by Laboratory for Molecular Medicine,Partners HealthCare Personalized Medicine

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Total variants: 34
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HGVS dbSNP
NM_000384.3(APOB):c.10556C>T (p.Thr3519Ile) rs746951119
NM_000384.3(APOB):c.10579C>T (p.Arg3527Trp) rs144467873
NM_000384.3(APOB):c.10580G>A (p.Arg3527Gln) rs5742904
NM_000384.3(APOB):c.10672C>T (p.Arg3558Cys) rs12713559
NM_000384.3(APOB):c.10708C>T (p.His3570Tyr) rs201736972
NM_000384.3(APOB):c.10913G>A (p.Arg3638Gln) rs1801701
NM_000384.3(APOB):c.11477C>T (p.Thr3826Met) rs61744153
NM_000384.3(APOB):c.11761G>A (p.Val3921Ile) rs72654409
NM_000384.3(APOB):c.1223T>C (p.Ile408Thr) rs12714225
NM_000384.3(APOB):c.13154G>A (p.Arg4385His) rs533755016
NM_000384.3(APOB):c.13181T>C (p.Val4394Ala) rs12720843
NM_000384.3(APOB):c.13288T>A (p.Ser4430Thr) rs72654426
NM_000384.3(APOB):c.2068-4T>A rs41291161
NM_000384.3(APOB):c.2914G>A (p.Gly972Ser) rs199893862
NM_000384.3(APOB):c.2981C>T (p.Pro994Leu) rs41288783
NM_000384.3(APOB):c.3337G>C (p.Asp1113His) rs12713844
NM_000384.3(APOB):c.3383G>A (p.Arg1128His) rs12713843
NM_000384.3(APOB):c.3427C>T (p.Pro1143Ser) rs72653077
NM_000384.3(APOB):c.5066G>A (p.Arg1689His) rs151009667
NM_000384.3(APOB):c.5599C>T (p.Arg1867Trp) rs200583769
NM_000384.3(APOB):c.5741A>G (p.Asn1914Ser) rs1801699
NM_000384.3(APOB):c.631C>T (p.Gln211Ter) rs143301836
NM_000384.3(APOB):c.6636_6638TGA[1] (p.Asp2213del) rs541497967
NM_000384.3(APOB):c.6655C>T (p.Arg2219Cys) rs141641980
NM_000384.3(APOB):c.6895G>C (p.Asp2299His) rs12713681
NM_000384.3(APOB):c.7285T>A (p.Ser2429Thr) rs72653092
NM_000384.3(APOB):c.7696G>A (p.Glu2566Lys) rs1801696
NM_000384.3(APOB):c.7698G>C (p.Glu2566Asp) rs149306841
NM_000384.3(APOB):c.7853T>C (p.Ile2618Thr) rs531273434
NM_000384.3(APOB):c.8462C>T (p.Pro2821Leu) rs72653095
NM_000384.3(APOB):c.8550T>G (p.Ile2850Met) rs148498577
NM_000384.3(APOB):c.9175C>T (p.Arg3059Cys) rs146377316
NM_000384.3(APOB):c.9639C>A (p.Asn3213Lys) rs574725520
NM_000384.3(APOB):c.9835A>G (p.Ser3279Gly) rs12720854

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