ClinVar Miner

List of variants in gene APOB reported by Laboratorium voor Moleculaire Diagnostiek Experimentele Vasculaire Geneeskunde, Academisch Medisch Centrum

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Gene type:
ClinVar version:
Total variants: 40
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HGVS dbSNP gnomAD frequency
NM_000384.3(APOB):c.10708C>T (p.His3570Tyr) rs201736972 0.00021
NM_000384.3(APOB):c.10700C>T (p.Thr3567Met) rs368278927 0.00009
NM_000384.3(APOB):c.10579C>T (p.Arg3527Trp) rs144467873 0.00006
NM_000384.3(APOB):c.10739A>G (p.Asn3580Ser) rs762028704 0.00004
NM_000384.3(APOB):c.1595G>A (p.Arg532Gln) rs753831464 0.00002
NM_000384.3(APOB):c.10633G>T (p.Glu3545Ter) rs759934326 0.00001
NM_000384.3(APOB):c.10657G>A (p.Glu3553Lys) rs763118165 0.00001
NM_000384.3(APOB):c.10808A>G (p.His3603Arg) rs370481987 0.00001
NM_000384.3(APOB):c.11854C>T (p.Arg3952Cys) rs535121944 0.00001
NM_000384.3(APOB):c.13154G>A (p.Arg4385His) rs533755016 0.00001
NM_000384.3(APOB):c.13160A>T (p.Glu4387Val) rs150412734 0.00001
NM_000384.3(APOB):c.10182G>T (p.Lys3394Asn) rs1382988295
NM_000384.3(APOB):c.10520G>C (p.Arg3507Pro) rs201156840
NM_000384.3(APOB):c.10580G>A (p.Arg3527Gln)
NM_000384.3(APOB):c.10580G>T (p.Arg3527Leu) rs5742904
NM_000384.3(APOB):c.10672C>T (p.Arg3558Cys)
NM_000384.3(APOB):c.10724G>A (p.Gly3575Asp) rs1418775778
NM_000384.3(APOB):c.10740C>G (p.Asn3580Lys) rs150312765
NM_000384.3(APOB):c.10768G>A (p.Glu3590Lys) rs747606537
NM_000384.3(APOB):c.10780T>C (p.Trp3594Arg)
NM_000384.3(APOB):c.10913G>A (p.Arg3638Gln)
NM_000384.3(APOB):c.13013G>A (p.Ser4338Asn)
NM_000384.3(APOB):c.13028_13029del (p.Tyr4343fs) rs760832994
NM_000384.3(APOB):c.13114C>T (p.Gln4372Ter) rs1442815965
NM_000384.3(APOB):c.13126C>T (p.Gln4376Ter) rs1553382326
NM_000384.3(APOB):c.13129_13130del (p.Ile4377fs) rs1553382325
NM_000384.3(APOB):c.13135C>T (p.Gln4379Ter) rs1553382319
NM_000384.3(APOB):c.13151T>C (p.Leu4384Pro) rs1339117465
NM_000384.3(APOB):c.13168G>C (p.Asp4390His) rs771015234
NM_000384.3(APOB):c.13196A>C (p.Lys4399Thr) rs1553382300
NM_000384.3(APOB):c.13220T>C (p.Ile4407Thr) rs1553382295
NM_000384.3(APOB):c.1594C>T (p.Arg532Trp)
NM_000384.3(APOB):c.2297_2298del (p.Lys766fs) rs1553385715
NM_000384.3(APOB):c.2786del (p.Pro929fs) rs1553385404
NM_000384.3(APOB):c.2786dup (p.Arg931fs) rs1553385404
NM_000384.3(APOB):c.3337G>C (p.Asp1113His)
NM_000384.3(APOB):c.3614_3625delinsCTTAGG (p.His1205_Asn1209delinsProTer) rs1553384441
NM_000384.3(APOB):c.4089C>G (p.Tyr1363Ter) rs1553384177
NM_000384.3(APOB):c.5238T>G (p.Tyr1746Ter) rs1553383898
NM_000384.3(APOB):c.9175C>T (p.Arg3059Cys)

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