ClinVar Miner

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

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 152
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_000384.3(APOB):c.10672C>T (p.Arg3558Cys) rs12713559 0.00050
NM_000384.3(APOB):c.895T>G (p.Phe299Val) rs72653060 0.00050
NM_000384.3(APOB):c.11720A>G (p.Asp3907Gly) rs61746686 0.00034
NM_000384.3(APOB):c.9322G>A (p.Glu3108Lys) rs140240214 0.00033
NM_000384.3(APOB):c.2411G>A (p.Arg804His) rs148190577 0.00028
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.10882A>T (p.Asn3628Tyr) rs141982176 0.00023
NM_000384.3(APOB):c.7181T>C (p.Val2394Ala) rs148429884 0.00023
NM_000384.3(APOB):c.925G>A (p.Ala309Thr) rs141888564 0.00022
NM_000384.3(APOB):c.13444A>G (p.Ile4482Val) rs142702699 0.00019
NM_000384.3(APOB):c.9811G>A (p.Gly3271Ser) rs142422341 0.00019
NM_000384.3(APOB):c.4532C>T (p.Thr1511Ile) rs146247063 0.00018
NM_000384.3(APOB):c.8882A>G (p.Asn2961Ser) rs142756262 0.00016
NM_000384.3(APOB):c.4970C>T (p.Thr1657Met) rs144239254 0.00015
NM_000384.3(APOB):c.6941T>C (p.Leu2314Pro) rs372035579 0.00015
NM_000384.3(APOB):c.2258G>A (p.Gly753Glu) rs148502464 0.00013
NM_000384.3(APOB):c.1010T>A (p.Ile337Asn) rs148126873 0.00012
NM_000384.3(APOB):c.2204T>A (p.Val735Glu) rs199872875 0.00011
NM_000384.3(APOB):c.400G>T (p.Ala134Ser) rs368321279 0.00011
NM_000384.3(APOB):c.890G>A (p.Arg297His) rs147223101 0.00011
NM_000384.3(APOB):c.11443G>A (p.Val3815Met) rs551178628 0.00010
NM_000384.3(APOB):c.11965C>T (p.Arg3989Cys) rs150713761 0.00010
NM_000384.3(APOB):c.5137G>T (p.Ala1713Ser) rs769789232 0.00010
NM_000384.3(APOB):c.10700C>T (p.Thr3567Met) rs368278927 0.00009
NM_000384.3(APOB):c.11816G>A (p.Gly3939Asp) rs142828185 0.00009
NM_000384.3(APOB):c.5044A>G (p.Met1682Val) rs140858817 0.00009
NM_000384.3(APOB):c.13288T>A (p.Ser4430Thr) rs72654426 0.00008
NM_000384.3(APOB):c.1295T>C (p.Met432Thr) rs371145776 0.00007
NM_000384.3(APOB):c.6655C>T (p.Arg2219Cys) rs141641980 0.00007
NM_000384.3(APOB):c.7094C>T (p.Ala2365Val) rs200034452 0.00007
NM_000384.3(APOB):c.10508C>T (p.Ser3503Leu) rs375284245 0.00006
NM_000384.3(APOB):c.5734A>T (p.Asn1912Tyr) rs186480094 0.00006
NM_000384.3(APOB):c.5863G>A (p.Val1955Met) rs368970025 0.00006
NM_000384.3(APOB):c.9407G>A (p.Arg3136His) rs199590149 0.00006
NM_000384.3(APOB):c.12731C>G (p.Ser4244Cys) rs1052000878 0.00005
NM_000384.3(APOB):c.6223G>A (p.Glu2075Lys) rs377429190 0.00005
NM_000384.3(APOB):c.9448T>C (p.Phe3150Leu) rs185224477 0.00005
NM_000384.3(APOB):c.1061A>G (p.Glu354Gly) rs149227065 0.00004
NM_000384.3(APOB):c.12536C>T (p.Thr4179Ile) rs370180297 0.00004
NM_000384.3(APOB):c.4441G>A (p.Val1481Ile) rs748985164 0.00004
NM_000384.3(APOB):c.6283G>A (p.Val2095Ile) rs200874264 0.00004
NM_000384.3(APOB):c.721A>T (p.Ser241Cys) rs758838678 0.00004
NM_000384.3(APOB):c.8531T>A (p.Leu2844Gln) rs776056927 0.00004
NM_000384.3(APOB):c.8608A>G (p.Ser2870Gly) rs373961682 0.00004
NM_000384.3(APOB):c.8720G>A (p.Arg2907His) rs751437976 0.00004
NM_000384.3(APOB):c.12148G>A (p.Glu4050Lys) rs201448956 0.00003
NM_000384.3(APOB):c.12765C>T (p.Phe4255=) rs746160756 0.00003
NM_000384.3(APOB):c.13566C>T (p.Asp4522=) rs371437581 0.00003
NM_000384.3(APOB):c.2170G>T (p.Gly724Cys) rs143425834 0.00003
NM_000384.3(APOB):c.2675C>T (p.Pro892Leu) rs780537483 0.00003
NM_000384.3(APOB):c.2728G>T (p.Gly910Cys) rs747610107 0.00003
NM_000384.3(APOB):c.2968G>A (p.Ala990Thr) rs139434026 0.00003
NM_000384.3(APOB):c.3595G>A (p.Asp1199Asn) rs375894411 0.00003
NM_000384.3(APOB):c.598G>A (p.Ala200Thr) rs763878189 0.00003
NM_000384.3(APOB):c.6100A>G (p.Ile2034Val) rs200339216 0.00003
NM_000384.3(APOB):c.7180G>T (p.Val2394Phe) rs775274391 0.00003
NM_000384.3(APOB):c.7565G>A (p.Arg2522Gln) rs781243278 0.00003
NM_000384.3(APOB):c.7853T>C (p.Ile2618Thr) rs531273434 0.00003
NM_000384.3(APOB):c.9803C>T (p.Ser3268Leu) rs755753053 0.00003
NM_000384.3(APOB):c.10945G>A (p.Glu3649Lys) rs754128155 0.00002
NM_000384.3(APOB):c.12890G>A (p.Arg4297His) rs375701380 0.00002
NM_000384.3(APOB):c.4927G>A (p.Ala1643Thr) rs774862312 0.00002
NM_000384.3(APOB):c.5882G>A (p.Ser1961Asn) rs974524838 0.00002
NM_000384.3(APOB):c.640C>T (p.Arg214Cys) rs763352655 0.00002
NM_000384.3(APOB):c.10318T>G (p.Phe3440Val) rs13306192 0.00001
NM_000384.3(APOB):c.11033C>T (p.Pro3678Leu) rs1278748798 0.00001
NM_000384.3(APOB):c.11071G>A (p.Asp3691Asn) rs149268579 0.00001
NM_000384.3(APOB):c.11261C>T (p.Thr3754Ile) rs139599466 0.00001
NM_000384.3(APOB):c.11597C>G (p.Ser3866Cys) rs748109934 0.00001
NM_000384.3(APOB):c.11925C>T (p.His3975=) rs771298370 0.00001
NM_000384.3(APOB):c.1213C>A (p.Pro405Thr) rs61745113 0.00001
NM_000384.3(APOB):c.12979A>T (p.Asn4327Tyr) rs755734023 0.00001
NM_000384.3(APOB):c.1309C>T (p.Arg437Cys) rs776786681 0.00001
NM_000384.3(APOB):c.13154G>A (p.Arg4385His) rs533755016 0.00001
NM_000384.3(APOB):c.13277T>C (p.Ile4426Thr) rs768381269 0.00001
NM_000384.3(APOB):c.13538T>G (p.Phe4513Cys) rs1231966626 0.00001
NM_000384.3(APOB):c.1827A>G (p.Gln609=) rs1038269557 0.00001
NM_000384.3(APOB):c.2635G>A (p.Val879Met) rs564030306 0.00001
NM_000384.3(APOB):c.2691T>G (p.Ser897Arg) rs144806800 0.00001
NM_000384.3(APOB):c.2722G>A (p.Glu908Lys) rs761179789 0.00001
NM_000384.3(APOB):c.3239A>G (p.Asn1080Ser) rs201825493 0.00001
NM_000384.3(APOB):c.339G>C (p.Leu113=) rs1367232226 0.00001
NM_000384.3(APOB):c.3671G>A (p.Arg1224Gln) rs530511188 0.00001
NM_000384.3(APOB):c.386A>G (p.Tyr129Cys) rs201368319 0.00001
NM_000384.3(APOB):c.4115C>T (p.Ser1372Phe) rs930883549 0.00001
NM_000384.3(APOB):c.4201T>C (p.Ser1401Pro) rs781141343 0.00001
NM_000384.3(APOB):c.4591A>C (p.Asn1531His) rs1169900515 0.00001
NM_000384.3(APOB):c.5406A>G (p.Lys1802=) rs201432579 0.00001
NM_000384.3(APOB):c.6002C>T (p.Thr2001Ile) rs763424475 0.00001
NM_000384.3(APOB):c.6035G>A (p.Arg2012Gln) rs749146264 0.00001
NM_000384.3(APOB):c.7346G>A (p.Arg2449Lys) rs576639442 0.00001
NM_000384.3(APOB):c.7374A>T (p.Glu2458Asp) rs766371877 0.00001
NM_000384.3(APOB):c.7446A>G (p.Glu2482=) rs1281732110 0.00001
NM_000384.3(APOB):c.7454A>G (p.Gln2485Arg) rs779284353 0.00001
NM_000384.3(APOB):c.7522A>G (p.Met2508Val) rs1206439836 0.00001
NM_000384.3(APOB):c.7939A>C (p.Thr2647Pro) rs748143305 0.00001
NM_000384.3(APOB):c.8719C>T (p.Arg2907Cys) rs745741960 0.00001
NM_000384.3(APOB):c.9698A>T (p.Tyr3233Phe) rs753419406 0.00001
NM_000384.3(APOB):c.10292C>A (p.Ala3431Asp) rs2103352011
NM_000384.3(APOB):c.10431T>G (p.Val3477=)
NM_000384.3(APOB):c.10660G>A (p.Ala3554Thr)
NM_000384.3(APOB):c.11116A>G (p.Thr3706Ala)
NM_000384.3(APOB):c.1168T>A (p.Cys390Ser)
NM_000384.3(APOB):c.1220_1270del (p.Leu407_Ala423del) rs2465432653
NM_000384.3(APOB):c.12226A>G (p.Lys4076Glu) rs2465351120
NM_000384.3(APOB):c.12334G>A (p.Ala4112Thr) rs1663036153
NM_000384.3(APOB):c.12412A>G (p.Thr4138Ala) rs2465350569
NM_000384.3(APOB):c.12443_12444delinsAA (p.Ala4148Glu) rs1558559244
NM_000384.3(APOB):c.12741A>G (p.Gln4247=)
NM_000384.3(APOB):c.12929T>C (p.Ile4310Thr) rs1003580237
NM_000384.3(APOB):c.13028_13029del (p.Tyr4343fs) rs760832994
NM_000384.3(APOB):c.13293C>A (p.Asn4431Lys) rs2465348156
NM_000384.3(APOB):c.13477CAG[1] (p.Gln4494del) rs562574661
NM_000384.3(APOB):c.13512C>A (p.Asp4504Glu)
NM_000384.3(APOB):c.13530T>C (p.Tyr4510=) rs753852142
NM_000384.3(APOB):c.13547A>C (p.Glu4516Ala)
NM_000384.3(APOB):c.1606C>G (p.Pro536Ala) rs760504695
NM_000384.3(APOB):c.1626G>T (p.Glu542Asp) rs367788462
NM_000384.3(APOB):c.1655C>A (p.Ala552Asp) rs765746519
NM_000384.3(APOB):c.1830-15CTT[2] rs764623841
NM_000384.3(APOB):c.1978A>G (p.Ile660Val)
NM_000384.3(APOB):c.2072G>T (p.Gly691Val) rs1572795241
NM_000384.3(APOB):c.2407G>A (p.Ala803Thr) rs757185314
NM_000384.3(APOB):c.2408C>T (p.Ala803Val) rs1663696423
NM_000384.3(APOB):c.263G>A (p.Cys88Tyr) rs1290557659
NM_000384.3(APOB):c.320C>T (p.Pro107Leu) rs1270615687
NM_000384.3(APOB):c.3379C>G (p.Pro1127Ala) rs539614975
NM_000384.3(APOB):c.395A>C (p.Lys132Thr) rs762667000
NM_000384.3(APOB):c.4056_4064dup (p.Gly1354_Leu1356dup) rs777844352
NM_000384.3(APOB):c.4240C>A (p.His1414Asn)
NM_000384.3(APOB):c.4411T>G (p.Leu1471Val) rs542169352
NM_000384.3(APOB):c.5234C>T (p.Ser1745Leu)
NM_000384.3(APOB):c.5689C>T (p.Arg1897Cys) rs189341276
NM_000384.3(APOB):c.6057A>G (p.Leu2019=) rs1663292441
NM_000384.3(APOB):c.682A>G (p.Ile228Val) rs2465445551
NM_000384.3(APOB):c.7347A>G (p.Arg2449=) rs1663246649
NM_000384.3(APOB):c.7466T>G (p.Ile2489Arg) rs2465368781
NM_000384.3(APOB):c.8045G>T (p.Ser2682Ile) rs375053331
NM_000384.3(APOB):c.8055G>T (p.Gln2685His) rs2465367278
NM_000384.3(APOB):c.8069A>G (p.Asp2690Gly)
NM_000384.3(APOB):c.816C>T (p.Tyr272=)
NM_000384.3(APOB):c.8181C>A (p.Asn2727Lys) rs958169216
NM_000384.3(APOB):c.8444C>T (p.Ser2815Leu)
NM_000384.3(APOB):c.8956C>T (p.Leu2986Phe) rs1472048923
NM_000384.3(APOB):c.9105T>G (p.Asn3035Lys) rs147510760
NM_000384.3(APOB):c.9110T>G (p.Leu3037Arg) rs1490729577
NM_000384.3(APOB):c.9149C>T (p.Thr3050Ile) rs766404863
NM_000384.3(APOB):c.9500A>C (p.Gln3167Pro)
NM_000384.3(APOB):c.9559A>T (p.Thr3187Ser)
NM_000384.3(APOB):c.9632A>C (p.Asn3211Thr) rs768051007
NM_000384.3(APOB):c.9867C>A (p.Asp3289Glu) rs72654404

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.