ClinVar Miner

List of variants in gene APOB reported as likely benign by Quest Diagnostics Nichols Institute San Juan Capistrano

Minimum submission review status: Collection method:
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Gene type:
ClinVar version:
Total variants: 58
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HGVS dbSNP gnomAD frequency
NM_000384.3(APOB):c.13369G>A (p.Asp4457Asn) rs183812948 0.00250
NM_000384.3(APOB):c.11833A>G (p.Thr3945Ala) rs1801698 0.00212
NM_000384.3(APOB):c.7615G>A (p.Val2539Ile) rs148170480 0.00210
NM_000384.3(APOB):c.11819C>T (p.Thr3940Met) rs72654416 0.00161
NM_000384.3(APOB):c.9226C>A (p.Leu3076Met) rs72653099 0.00129
NM_000384.3(APOB):c.4838G>C (p.Ser1613Thr) rs61742247 0.00093
NM_000384.3(APOB):c.9937C>A (p.Leu3313Ile) rs146687604 0.00088
NM_000384.3(APOB):c.13102C>G (p.Gln4368Glu) rs72654424 0.00080
NM_000384.3(APOB):c.641G>A (p.Arg214His) rs146152405 0.00064
NM_000384.3(APOB):c.285C>A (p.Ser95Arg) rs143613534 0.00058
NM_000384.3(APOB):c.12348T>C (p.Tyr4116=) rs143685680 0.00056
NM_000384.3(APOB):c.12784C>T (p.Leu4262=) rs12713457 0.00044
NM_000384.3(APOB):c.7152T>C (p.Val2384=) rs72653090 0.00041
NM_000384.3(APOB):c.5811T>C (p.Pro1937=) rs141657364 0.00032
NM_000384.3(APOB):c.2853G>A (p.Glu951=) rs151193347 0.00031
NM_000384.3(APOB):c.2268C>T (p.Leu756=) rs181882915 0.00028
NM_000384.3(APOB):c.9810C>T (p.Phe3270=) rs138010392 0.00027
NM_000384.3(APOB):c.9883T>C (p.Tyr3295His) rs186299244 0.00027
NM_000384.3(APOB):c.11820G>A (p.Thr3940=) rs72654417 0.00024
NM_000384.3(APOB):c.5763A>G (p.Gly1921=) rs141022509 0.00023
NM_000384.3(APOB):c.7863A>C (p.Leu2621=) rs138497378 0.00022
NM_000384.3(APOB):c.10708C>T (p.His3570Tyr) rs201736972 0.00021
NM_000384.3(APOB):c.2988C>T (p.Thr996=) rs137875230 0.00021
NM_000384.3(APOB):c.12016G>A (p.Val4006Ile) rs183117027 0.00019
NM_000384.3(APOB):c.7331G>A (p.Arg2444His) rs200143030 0.00019
NM_000384.3(APOB):c.2313G>A (p.Pro771=) rs552986140 0.00009
NM_000384.3(APOB):c.3471T>C (p.Tyr1157=) rs201128198 0.00009
NM_000384.3(APOB):c.7998A>G (p.Val2666=) rs1042006 0.00007
NM_000384.3(APOB):c.10371C>T (p.Ser3457=) rs139891446 0.00005
NM_000384.3(APOB):c.12381C>T (p.Asp4127=) rs145704672 0.00005
NM_000384.3(APOB):c.11319G>A (p.Lys3773=) rs780811733 0.00004
NM_000384.3(APOB):c.11789-8C>T rs201274370 0.00004
NM_000384.3(APOB):c.4251G>A (p.Thr1417=) rs72653082 0.00004
NM_000384.3(APOB):c.4257A>G (p.Thr1419=) rs778729560 0.00004
NM_000384.3(APOB):c.11787T>C (p.Asn3929=) rs1047501521 0.00003
NM_000384.3(APOB):c.12510C>T (p.Asn4170=) rs764649432 0.00001
NM_000384.3(APOB):c.2556A>C (p.Gly852=) rs778199079 0.00001
NM_000384.3(APOB):c.7554T>C (p.Asp2518=) rs768488788 0.00001
NM_000384.3(APOB):c.8724C>T (p.Asn2908=) rs755498745 0.00001
NM_000384.3(APOB):c.9195A>G (p.Thr3065=) rs749791220 0.00001
NM_000384.3(APOB):c.9930T>C (p.Pro3310=) rs764448582 0.00001
NM_000384.3(APOB):c.11401T>A (p.Ser3801Thr)
NM_000384.3(APOB):c.11477C>T (p.Thr3826Met)
NM_000384.3(APOB):c.11478G>A (p.Thr3826=)
NM_000384.3(APOB):c.1310G>A (p.Arg437His)
NM_000384.3(APOB):c.2478T>C (p.Phe826=) rs377697247
NM_000384.3(APOB):c.307T>C (p.Tyr103His)
NM_000384.3(APOB):c.3122-6G>A rs72653071
NM_000384.3(APOB):c.3427C>T (p.Pro1143Ser)
NM_000384.3(APOB):c.4663A>G (p.Ile1555Val)
NM_000384.3(APOB):c.4676C>T (p.Ala1559Val) rs549741449
NM_000384.3(APOB):c.4754A>T (p.Asn1585Ile) rs549983245
NM_000384.3(APOB):c.5066G>A (p.Arg1689His)
NM_000384.3(APOB):c.594T>C (p.Asn198=)
NM_000384.3(APOB):c.6021G>C (p.Val2007=) rs148252000
NM_000384.3(APOB):c.7285T>A (p.Ser2429Thr)
NM_000384.3(APOB):c.7965C>T (p.Thr2655=)
NM_000384.3(APOB):c.9242G>A (p.Ser3081Asn) rs72653100

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