ClinVar Miner

List of variants in gene APOB reported as uncertain significance by Invitae

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Total variants: 123
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HGVS dbSNP
NM_000384.3(APOB):c.10025C>T (p.Ser3342Phe) rs267599180
NM_000384.3(APOB):c.10032A>C (p.Lys3344Asn) rs757857092
NM_000384.3(APOB):c.1010T>A (p.Ile337Asn)
NM_000384.3(APOB):c.10146G>C (p.Glu3382Asp) rs1558561585
NM_000384.3(APOB):c.10240G>A (p.Val3414Met) rs749800586
NM_000384.3(APOB):c.10276G>A (p.Ala3426Thr) rs753767897
NM_000384.3(APOB):c.10520G>C (p.Arg3507Pro) rs201156840
NM_000384.3(APOB):c.10571A>C (p.Lys3524Thr) rs750035232
NM_000384.3(APOB):c.10672C>T (p.Arg3558Cys) rs12713559
NM_000384.3(APOB):c.10678T>C (p.Tyr3560His) rs1558561174
NM_000384.3(APOB):c.10679A>G (p.Tyr3560Cys) rs745721296
NM_000384.3(APOB):c.10777C>G (p.Pro3593Ala)
NM_000384.3(APOB):c.1077T>G (p.Ser359Arg)
NM_000384.3(APOB):c.10825T>A (p.Ser3609Thr) rs1060500239
NM_000384.3(APOB):c.10876A>G (p.Thr3626Ala) rs1553382890
NM_000384.3(APOB):c.11233G>A (p.Val3745Ile) rs147564959
NM_000384.3(APOB):c.11285A>C (p.Lys3762Thr)
NM_000384.3(APOB):c.11911G>A (p.Glu3971Lys) rs373477107
NM_000384.3(APOB):c.11966G>A (p.Arg3989His) rs148197354
NM_000384.3(APOB):c.12038T>C (p.Met4013Thr) rs144922840
NM_000384.3(APOB):c.12112A>G (p.Ile4038Val) rs1443981616
NM_000384.3(APOB):c.12220G>A (p.Val4074Met) rs1038411462
NM_000384.3(APOB):c.12298G>A (p.Val4100Met)
NM_000384.3(APOB):c.12343G>A (p.Val4115Ile) rs765681925
NM_000384.3(APOB):c.12416G>A (p.Gly4139Glu) rs1558559266
NM_000384.3(APOB):c.12457C>A (p.Gln4153Lys) rs1228367728
NM_000384.3(APOB):c.12529C>A (p.Arg4177=) rs375275230
NM_000384.3(APOB):c.12536C>T (p.Thr4179Ile) rs370180297
NM_000384.3(APOB):c.12724C>A (p.Leu4242Met)
NM_000384.3(APOB):c.12739C>T (p.Gln4247Ter) rs907126709
NM_000384.3(APOB):c.12977T>A (p.Ile4326Asn)
NM_000384.3(APOB):c.13101del (p.Gln4368fs)
NM_000384.3(APOB):c.13175G>A (p.Ser4392Asn) rs777718986
NM_000384.3(APOB):c.13181T>C (p.Val4394Ala) rs12720843
NM_000384.3(APOB):c.13183G>A (p.Gly4395Ser) rs151333262
NM_000384.3(APOB):c.13448C>T (p.Ala4483Val) rs147416761
NM_000384.3(APOB):c.13477_13479CAG[1] (p.Gln4494del) rs562574661
NM_000384.3(APOB):c.1400C>G (p.Ala467Gly) rs376602710
NM_000384.3(APOB):c.1472T>C (p.Val491Ala)
NM_000384.3(APOB):c.1554G>C (p.Lys518Asn)
NM_000384.3(APOB):c.1562T>G (p.Leu521Arg)
NM_000384.3(APOB):c.1577C>T (p.Ala526Val) rs1558572895
NM_000384.3(APOB):c.1993A>T (p.Asn665Tyr) rs755666654
NM_000384.3(APOB):c.2386G>C (p.Gly796Arg)
NM_000384.3(APOB):c.2414C>G (p.Thr805Ser) rs1291440333
NM_000384.3(APOB):c.2585T>C (p.Val862Ala) rs145142090
NM_000384.3(APOB):c.2657A>G (p.Asn886Ser) rs183398286
NM_000384.3(APOB):c.2675C>T (p.Pro892Leu) rs780537483
NM_000384.3(APOB):c.2849C>T (p.Thr950Met)
NM_000384.3(APOB):c.2938G>A (p.Ala980Thr) rs369310292
NM_000384.3(APOB):c.2968G>A (p.Ala990Thr) rs139434026
NM_000384.3(APOB):c.2978A>G (p.Tyr993Cys)
NM_000384.3(APOB):c.318C>G (p.Asn106Lys) rs371662800
NM_000384.3(APOB):c.3283G>A (p.Asp1095Asn) rs1377332778
NM_000384.3(APOB):c.3583G>A (p.Val1195Met) rs1060500236
NM_000384.3(APOB):c.3617T>C (p.Met1206Thr) rs878853972
NM_000384.3(APOB):c.3717G>T (p.Gln1239His)
NM_000384.3(APOB):c.4024A>G (p.Ile1342Val) rs780328279
NM_000384.3(APOB):c.4039C>G (p.Gln1347Glu)
NM_000384.3(APOB):c.4056_4064dup (p.Gly1354_Leu1356dup) rs777844352
NM_000384.3(APOB):c.413G>A (p.Gly138Glu)
NM_000384.3(APOB):c.4265G>A (p.Cys1422Tyr) rs568413
NM_000384.3(APOB):c.4280G>A (p.Arg1427His) rs145324793
NM_000384.3(APOB):c.434C>T (p.Pro145Leu) rs181737266
NM_000384.3(APOB):c.4544A>G (p.Asn1515Ser)
NM_000384.3(APOB):c.4586G>A (p.Gly1529Asp) rs558304720
NM_000384.3(APOB):c.4850G>A (p.Gly1617Glu)
NM_000384.3(APOB):c.4983G>C (p.Lys1661Asn)
NM_000384.3(APOB):c.5057C>T (p.Thr1686Ile) rs1060500240
NM_000384.3(APOB):c.5137G>T (p.Ala1713Ser)
NM_000384.3(APOB):c.522G>C (p.Lys174Asn)
NM_000384.3(APOB):c.5269C>G (p.Leu1757Val) rs1315014976
NM_000384.3(APOB):c.5599C>T (p.Arg1867Trp) rs200583769
NM_000384.3(APOB):c.5608A>G (p.Thr1870Ala)
NM_000384.3(APOB):c.5722G>A (p.Asp1908Asn)
NM_000384.3(APOB):c.574G>A (p.Val192Ile) rs200662943
NM_000384.3(APOB):c.5822C>T (p.Thr1941Ile)
NM_000384.3(APOB):c.5989G>A (p.Asp1997Asn)
NM_000384.3(APOB):c.598G>A (p.Ala200Thr)
NM_000384.3(APOB):c.6018C>T (p.Gly2006=) rs368422207
NM_000384.3(APOB):c.6070A>G (p.Ile2024Val) rs564588440
NM_000384.3(APOB):c.6092G>C (p.Ser2031Thr) rs776946940
NM_000384.3(APOB):c.6443A>T (p.Lys2148Met)
NM_000384.3(APOB):c.6606_6608TGA[1] (p.Asp2203del) rs1060500238
NM_000384.3(APOB):c.6698T>C (p.Ile2233Thr)
NM_000384.3(APOB):c.689G>T (p.Gly230Val) rs755661819
NM_000384.3(APOB):c.6974T>C (p.Ile2325Thr)
NM_000384.3(APOB):c.7036G>A (p.Glu2346Lys) rs769939347
NM_000384.3(APOB):c.7201G>C (p.Val2401Leu) rs569794936
NM_000384.3(APOB):c.7209G>T (p.Lys2403Asn) rs777497625
NM_000384.3(APOB):c.721A>T (p.Ser241Cys)
NM_000384.3(APOB):c.7648A>G (p.Ile2550Val) rs147565300
NM_000384.3(APOB):c.7727G>A (p.Arg2576His)
NM_000384.3(APOB):c.7759G>C (p.Val2587Leu)
NM_000384.3(APOB):c.7823A>C (p.Gln2608Pro)
NM_000384.3(APOB):c.7843C>T (p.Pro2615Ser)
NM_000384.3(APOB):c.7853T>C (p.Ile2618Thr) rs531273434
NM_000384.3(APOB):c.7976C>T (p.Pro2659Leu) rs922450819
NM_000384.3(APOB):c.8134C>T (p.Arg2712Cys) rs372245645
NM_000384.3(APOB):c.8187_8193delinsAGATTTA (p.Asn2729_Phe2731delinsLysAspLeu) rs1553383380
NM_000384.3(APOB):c.8243A>G (p.His2748Arg)
NM_000384.3(APOB):c.8294A>G (p.Gln2765Arg)
NM_000384.3(APOB):c.8499G>C (p.Lys2833Asn) rs761515806
NM_000384.3(APOB):c.8550T>G (p.Ile2850Met) rs148498577
NM_000384.3(APOB):c.8693T>C (p.Leu2898Pro) rs376974746
NM_000384.3(APOB):c.8720G>A (p.Arg2907His) rs751437976
NM_000384.3(APOB):c.8855G>T (p.Gly2952Val)
NM_000384.3(APOB):c.8882A>G (p.Asn2961Ser) rs142756262
NM_000384.3(APOB):c.890G>A (p.Arg297His)
NM_000384.3(APOB):c.9077A>T (p.Asn3026Ile)
NM_000384.3(APOB):c.9080G>A (p.Gly3027Glu) rs757895045
NM_000384.3(APOB):c.9145T>A (p.Ser3049Thr)
NM_000384.3(APOB):c.9175C>T (p.Arg3059Cys) rs146377316
NM_000384.3(APOB):c.9200A>T (p.Lys3067Met) rs1558562275
NM_000384.3(APOB):c.9221A>G (p.Tyr3074Cys) rs372902533
NM_000384.3(APOB):c.925G>A (p.Ala309Thr) rs141888564
NM_000384.3(APOB):c.9385C>G (p.Pro3129Ala) rs143933265
NM_000384.3(APOB):c.9633C>A (p.Asn3211Lys) rs748318755
NM_000384.3(APOB):c.9712T>A (p.Ser3238Thr)
NM_000384.3(APOB):c.9721G>A (p.Glu3241Lys) rs139245086
NM_000384.3(APOB):c.9738T>G (p.Phe3246Leu)
NM_000384.3(APOB):c.9770A>G (p.Asn3257Ser)
NM_000384.3(APOB):c.9788T>C (p.Phe3263Ser)

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