ClinVar Miner

List of variants in gene APOB reported by Division of Genomic Diagnostics,The Children's Hospital of Philadelphia

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Total variants: 24
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HGVS dbSNP
NM_000384.2(APOB):c.11477C>T (p.Thr3826Met) rs61744153
NM_000384.2(APOB):c.12766G>A (p.Glu4256Lys) rs61743313
NM_000384.2(APOB):c.12940A>G (p.Ile4314Val) rs72654423
NM_000384.2(APOB):c.1310G>A (p.Arg437His) rs142114415
NM_000384.2(APOB):c.13153C>T (p.Arg4385Cys) rs864309556
NM_000384.2(APOB):c.13441G>A (p.Ala4481Thr) rs1801695
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.3337G>C (p.Asp1113His) rs12713844
NM_000384.2(APOB):c.3362A>G (p.Lys1121Arg) rs879255342
NM_000384.2(APOB):c.3634C>A (p.Leu1212Met) rs61736761
NM_000384.2(APOB):c.3670C>T (p.Arg1224Trp) rs148959244
NM_000384.2(APOB):c.3724T>A (p.Ser1242Thr) rs200261177
NM_000384.2(APOB):c.4027C>T (p.Pro1343Ser) rs374427541
NM_000384.2(APOB):c.4178C>T (p.Ala1393Val) rs143282164
NM_000384.2(APOB):c.5741A>G (p.Asn1914Ser) rs1801699
NM_000384.2(APOB):c.574G>A (p.Val192Ile) rs200662943
NM_000384.2(APOB):c.5768A>G (p.His1923Arg) rs533617
NM_000384.2(APOB):c.6895G>C (p.Asp2299His) rs12713681
NM_000384.2(APOB):c.7285T>A (p.Ser2429Thr) rs72653092
NM_000384.2(APOB):c.7721C>T (p.Ala2574Val) rs150843941
NM_000384.2(APOB):c.8353A>C (p.Asn2785His) rs2163204
NM_000384.2(APOB):c.8462C>T (p.Pro2821Leu) rs72653095
NM_000384.2(APOB):c.9835A>G (p.Ser3279Gly) rs12720854

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