ClinVar Miner

List of variants in gene APC 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: 108
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HGVS dbSNP gnomAD frequency
NM_000038.6(APC):c.1240C>T (p.Arg414Cys) rs137854567 0.00053
NM_000038.6(APC):c.7490C>T (p.Ser2497Leu) rs141010008 0.00031
NM_000038.6(APC):c.2593C>T (p.Pro865Ser) rs192620988 0.00028
NM_000038.6(APC):c.8266A>G (p.Ile2756Val) rs146115809 0.00026
NM_000038.6(APC):c.6782C>T (p.Pro2261Leu) rs376494248 0.00021
NM_000038.6(APC):c.3374T>C (p.Val1125Ala) rs377278397 0.00018
NM_000038.6(APC):c.4237A>G (p.Met1413Val) rs141519952 0.00018
NM_000038.6(APC):c.5009C>T (p.Ala1670Val) rs202228932 0.00018
NM_000038.6(APC):c.6637A>G (p.Met2213Val) rs186926737 0.00018
NM_000038.6(APC):c.3479C>A (p.Thr1160Lys) rs201004111 0.00017
NM_000038.6(APC):c.7193C>T (p.Ser2398Phe) rs150882838 0.00017
NM_000038.6(APC):c.7625A>G (p.Asn2542Ser) rs151163793 0.00016
NM_000038.6(APC):c.7109G>T (p.Gly2370Val) rs140079759 0.00014
NM_000038.6(APC):c.1631T>C (p.Ile544Thr) rs144056494 0.00012
NM_000038.6(APC):c.2204C>T (p.Ala735Val) rs147655929 0.00012
NM_000038.6(APC):c.5392A>G (p.Asn1798Asp) rs200794097 0.00012
NM_000038.6(APC):c.5801C>T (p.Pro1934Leu) rs587780600 0.00012
NM_000038.6(APC):c.6873A>T (p.Gln2291His) rs148878262 0.00012
NM_000038.6(APC):c.3875C>T (p.Thr1292Met) rs371113837 0.00011
NM_000038.6(APC):c.573T>C (p.Tyr191=) rs185154886 0.00008
NM_000038.6(APC):c.4533C>T (p.Leu1511=) rs150089434 0.00007
NM_000038.6(APC):c.1139G>A (p.Arg380Gln) rs587782886 0.00006
NM_000038.6(APC):c.5140G>A (p.Asp1714Asn) rs148275069 0.00006
NM_000038.6(APC):c.5774C>A (p.Pro1925His) rs762682111 0.00006
NM_000038.6(APC):c.7399C>A (p.Pro2467Thr) rs372305287 0.00006
NM_000038.6(APC):c.7574G>A (p.Arg2525His) rs762034315 0.00006
NM_000038.6(APC):c.2438A>G (p.Asn813Ser) rs201522866 0.00005
NM_000038.6(APC):c.1242C>T (p.Arg414=) rs751423790 0.00004
NM_000038.6(APC):c.4416A>T (p.Val1472=) rs773352404 0.00004
NM_000038.6(APC):c.5571A>C (p.Ser1857=) rs376624613 0.00004
NM_000038.6(APC):c.6135C>T (p.Ser2045=) rs187297940 0.00004
NM_000038.6(APC):c.8061A>G (p.Ser2687=) rs746180965 0.00004
NM_000038.6(APC):c.1405C>T (p.Leu469=) rs746293695 0.00003
NM_000038.6(APC):c.2946G>A (p.Ser982=) rs377384463 0.00003
NM_000038.6(APC):c.385G>C (p.Glu129Gln) rs376628500 0.00003
NM_000038.6(APC):c.4525C>T (p.Leu1509=) rs572839648 0.00003
NM_000038.6(APC):c.6750C>T (p.Gly2250=) rs555799753 0.00003
NM_000038.6(APC):c.7209G>A (p.Gln2403=) rs769603145 0.00003
NM_000038.6(APC):c.7278A>G (p.Gly2426=) rs756770951 0.00003
NM_000038.6(APC):c.757G>A (p.Gly253Ser) rs772806807 0.00003
NM_000038.6(APC):c.8010A>G (p.Arg2670=) rs786201524 0.00003
NM_000038.6(APC):c.1158A>G (p.Ala386=) rs370669642 0.00002
NM_000038.6(APC):c.1272G>A (p.Gln424=) rs778975532 0.00002
NM_000038.6(APC):c.1313-9A>G rs368494354 0.00002
NM_000038.6(APC):c.1713A>G (p.Ala571=) rs529306174 0.00002
NM_000038.6(APC):c.480T>A (p.Ala160=) rs758296324 0.00002
NM_000038.6(APC):c.5363G>A (p.Arg1788His) rs201472075 0.00002
NM_000038.6(APC):c.5424C>T (p.Asn1808=) rs747721259 0.00002
NM_000038.6(APC):c.5823A>G (p.Pro1941=) rs770869007 0.00002
NM_000038.6(APC):c.6837A>G (p.Lys2279=) rs1057521763 0.00002
NM_000038.6(APC):c.6885A>G (p.Ser2295=) rs763506865 0.00002
NM_000038.6(APC):c.7443T>A (p.Thr2481=) rs147757080 0.00002
NM_000038.6(APC):c.948T>C (p.Tyr316=) rs748010172 0.00002
NM_000038.6(APC):c.1359A>G (p.Leu453=) rs751945983 0.00001
NM_000038.6(APC):c.1863T>C (p.Thr621=) rs72541808 0.00001
NM_000038.6(APC):c.1958+7A>G rs1057524097 0.00001
NM_000038.6(APC):c.2433A>G (p.Ser811=) rs768177978 0.00001
NM_000038.6(APC):c.2568C>T (p.Arg856=) rs751433216 0.00001
NM_000038.6(APC):c.2613A>C (p.Gly871=) rs36046448 0.00001
NM_000038.6(APC):c.2631T>A (p.Gly877=) rs762629631 0.00001
NM_000038.6(APC):c.2745G>A (p.Val915=) rs761286097 0.00001
NM_000038.6(APC):c.2958T>C (p.Tyr986=) rs746581330 0.00001
NM_000038.6(APC):c.3183A>G (p.Lys1061=) rs1580632127 0.00001
NM_000038.6(APC):c.3258C>T (p.His1086=) rs778031876 0.00001
NM_000038.6(APC):c.3378C>G (p.Ser1126Arg) rs149353082 0.00001
NM_000038.6(APC):c.3512G>A (p.Arg1171His) rs372481703 0.00001
NM_000038.6(APC):c.3555A>G (p.Thr1185=) rs786201125 0.00001
NM_000038.6(APC):c.372A>G (p.Val124=) rs749179034 0.00001
NM_000038.6(APC):c.3798T>C (p.Asp1266=) rs1488397941 0.00001
NM_000038.6(APC):c.4344C>T (p.Thr1448=) rs864622562 0.00001
NM_000038.6(APC):c.5670A>G (p.Ser1890=) rs945185629 0.00001
NM_000038.6(APC):c.6168C>G (p.Leu2056=) rs878853461 0.00001
NM_000038.6(APC):c.6504A>C (p.Leu2168=) rs750058868 0.00001
NM_000038.6(APC):c.6684G>A (p.Arg2228=) rs752314977 0.00001
NM_000038.6(APC):c.672C>T (p.Ile224=) rs367816013 0.00001
NM_000038.6(APC):c.7125A>G (p.Gln2375=) rs587780603 0.00001
NM_000038.6(APC):c.7194C>T (p.Ser2398=) rs565688379 0.00001
NM_000038.6(APC):c.7395T>C (p.Leu2465=) rs369906346 0.00001
NM_000038.6(APC):c.7533C>T (p.Leu2511=) rs1057522957 0.00001
NM_000038.6(APC):c.7645C>T (p.Arg2549Cys) rs199539353 0.00001
NM_000038.6(APC):c.8145C>T (p.Thr2715=) rs1554088935 0.00001
NM_000038.6(APC):c.8226A>G (p.Gln2742=) rs1404406885 0.00001
NM_000038.6(APC):c.*2AG[4] rs758692443
NM_000038.6(APC):c.1491A>G (p.Leu497=) rs201992951
NM_000038.6(APC):c.1656T>G (p.Ser552=) rs1554082105
NM_000038.6(APC):c.1692A>C (p.Arg564=) rs763295800
NM_000038.6(APC):c.2469A>G (p.Ser823=)
NM_000038.6(APC):c.2547T>C (p.Asp849=) rs766086010
NM_000038.6(APC):c.3510A>G (p.Lys1170=) rs786203746
NM_000038.6(APC):c.3774A>G (p.Thr1258=) rs542928573
NM_000038.6(APC):c.4200G>A (p.Ser1400=) rs367782881
NM_000038.6(APC):c.4200G>C (p.Ser1400=) rs367782881
NM_000038.6(APC):c.4260C>A (p.Pro1420=) rs770579741
NM_000038.6(APC):c.4317T>A (p.Pro1439=) rs769586752
NM_000038.6(APC):c.4512C>G (p.Ser1504=) rs999881274
NM_000038.6(APC):c.4524T>C (p.Ala1508=) rs767025305
NM_000038.6(APC):c.4962T>C (p.Ala1654=) rs551322279
NM_000038.6(APC):c.5268T>A (p.Ser1756=) rs866006
NM_000038.6(APC):c.6012A>G (p.Ala2004=) rs1057521822
NM_000038.6(APC):c.6162A>G (p.Ser2054=) rs776160547
NM_000038.6(APC):c.6354TGC[5] (p.Ala2122dup) rs587780602
NM_000038.6(APC):c.6474C>A (p.Pro2158=) rs772027192
NM_000038.6(APC):c.6474C>T (p.Pro2158=) rs772027192
NM_000038.6(APC):c.6579A>G (p.Lys2193=) rs908184283
NM_000038.6(APC):c.7026A>G (p.Leu2342=) rs766086022
NM_000038.6(APC):c.7308A>G (p.Val2436=) rs1220693522
NM_000038.6(APC):c.7536T>C (p.Ser2512=) rs587780604
NM_000038.6(APC):c.8148G>C (p.Val2716=) rs1158207177

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