ClinVar Miner

List of variants in gene CHEK2 reported as likely benign by Color

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Gene type:
ClinVar version:
Total variants: 176
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HGVS dbSNP
NM_007194.4(CHEK2):c.*16C>T rs1057522648
NM_007194.4(CHEK2):c.*18C>T rs17884403
NM_007194.4(CHEK2):c.*2dup rs749257861
NM_007194.4(CHEK2):c.*6G>A rs775315910
NM_007194.4(CHEK2):c.*7T>C rs121908710
NM_007194.4(CHEK2):c.-4C>T rs374938148
NM_007194.4(CHEK2):c.-6-8T>G rs1555932995
NM_007194.4(CHEK2):c.-6G>A rs376995740
NM_007194.4(CHEK2):c.1008+13C>T rs193264230
NM_007194.4(CHEK2):c.1008+15C>G rs1555915284
NM_007194.4(CHEK2):c.1008+8A>G rs139986197
NM_007194.4(CHEK2):c.1009-14G>C rs1172442364
NM_007194.4(CHEK2):c.1009-16C>A rs751749563
NM_007194.4(CHEK2):c.1009-20A>G rs946179247
NM_007194.4(CHEK2):c.1023C>T (p.Asn341=) rs377668478
NM_007194.4(CHEK2):c.1035C>T (p.His345=) rs756520206
NM_007194.4(CHEK2):c.1083C>T (p.Asp361=) rs572668197
NM_007194.4(CHEK2):c.1089T>C (p.Leu363=) rs761681864
NM_007194.4(CHEK2):c.1095+19G>A rs200020484
NM_007194.4(CHEK2):c.1095+8A>G rs1057522814
NM_007194.4(CHEK2):c.1096-10T>C rs1555913946
NM_007194.4(CHEK2):c.1096-16T>C rs1377212608
NM_007194.4(CHEK2):c.1096-4T>C rs587782840
NM_007194.4(CHEK2):c.1113C>T (p.His371=) rs876659094
NM_007194.4(CHEK2):c.1176G>A (p.Ala392=) rs142692907
NM_007194.4(CHEK2):c.1197T>C (p.Val399=) rs1057520268
NM_007194.4(CHEK2):c.1203T>C (p.Thr401=) rs560781587
NM_007194.4(CHEK2):c.1215C>A (p.Asn405Lys) rs587780171
NM_007194.4(CHEK2):c.1217G>A (p.Arg406His) rs200649225
NM_007194.4(CHEK2):c.1259+14T>A rs780245762
NM_007194.4(CHEK2):c.1259+14T>C rs780245762
NM_007194.4(CHEK2):c.1259+16A>G rs756361647
NM_007194.4(CHEK2):c.1259+17T>C rs746109434
NM_007194.4(CHEK2):c.1259+8A>G rs368388249
NM_007194.4(CHEK2):c.1260-18C>G rs1057521375
NM_007194.4(CHEK2):c.1260-18C>T rs1057521375
NM_007194.4(CHEK2):c.1260-20CT[3] rs760037989
NM_007194.4(CHEK2):c.1260-6del rs878854912
NM_007194.4(CHEK2):c.1284T>C (p.Ser428=) rs781514295
NM_007194.4(CHEK2):c.1287G>A (p.Glu429=) rs758102180
NM_007194.4(CHEK2):c.1323C>T (p.Thr441=) rs753839004
NM_007194.4(CHEK2):c.132C>T (p.Ser44=) rs199715101
NM_007194.4(CHEK2):c.135G>A (p.Thr45=) rs745423387
NM_007194.4(CHEK2):c.1375+17del rs1191159078
NM_007194.4(CHEK2):c.1377T>C (p.Ala459=) rs786201296
NM_007194.4(CHEK2):c.1386T>C (p.Leu462=) rs876659337
NM_007194.4(CHEK2):c.1407G>A (p.Val469=) rs17881378
NM_007194.4(CHEK2):c.1410T>C (p.Asp470=) rs864622382
NM_007194.4(CHEK2):c.1428G>A (p.Thr476=) rs1060504697
NM_007194.4(CHEK2):c.1452G>A (p.Pro484=) rs749156425
NM_007194.4(CHEK2):c.1461+3G>A rs1555913067
NM_007194.4(CHEK2):c.1461+4G>A rs1057522400
NM_007194.4(CHEK2):c.1461+8T>C rs1057521960
NM_007194.4(CHEK2):c.1462-20T>C rs747767986
NM_007194.4(CHEK2):c.1462-7C>G rs730881707
NM_007194.4(CHEK2):c.1489G>A (p.Asp497Asn) rs143965148
NM_007194.4(CHEK2):c.1491T>C (p.Asp497=) rs762041905
NM_007194.4(CHEK2):c.1494T>C (p.Leu498=) rs531931623
NM_007194.4(CHEK2):c.1497G>C (p.Leu499=) rs587780890
NM_007194.4(CHEK2):c.14C>T (p.Ser5Leu) rs201084748
NM_007194.4(CHEK2):c.1500T>C (p.Ser500=) rs1057521300
NM_007194.4(CHEK2):c.1501G>A (p.Glu501Lys) rs17883172
NM_007194.4(CHEK2):c.1503G>A (p.Glu501=) rs1060502721
NM_007194.4(CHEK2):c.150C>T (p.Ser50=) rs967317594
NM_007194.4(CHEK2):c.1510G>C (p.Glu504Gln) rs587782489
NM_007194.4(CHEK2):c.1525C>T (p.Pro509Ser) rs587780179
NM_007194.4(CHEK2):c.1526C>T (p.Pro509Leu) rs587782541
NM_007194.4(CHEK2):c.1534C>G (p.Leu512Val) rs17882942
NM_007194.4(CHEK2):c.1542+11T>C rs17881716
NM_007194.4(CHEK2):c.1542+6C>T rs1414780425
NM_007194.4(CHEK2):c.1542+7G>A rs4035547
NM_007194.4(CHEK2):c.1543-10T>C rs1555911654
NM_007194.4(CHEK2):c.1543-12C>G rs1555911657
NM_007194.4(CHEK2):c.1563G>A (p.Arg521=) rs761278013
NM_007194.4(CHEK2):c.156C>G (p.Ser52=) rs1555932466
NM_007194.4(CHEK2):c.1581C>T (p.Ala527=) rs781593101
NM_007194.4(CHEK2):c.1590C>T (p.Ala530=) rs786201796
NM_007194.4(CHEK2):c.1593G>A (p.Glu531=) rs758555487
NM_007194.4(CHEK2):c.1597A>G (p.Thr533Ala) rs562517792
NM_007194.4(CHEK2):c.15G>A (p.Ser5=) rs145183886
NM_007194.4(CHEK2):c.1602G>A (p.Lys534=) rs1569102099
NM_007194.4(CHEK2):c.1604G>A (p.Arg535His) rs544216926
NM_007194.4(CHEK2):c.1623T>C (p.Ala541=) rs773670297
NM_007194.4(CHEK2):c.171T>C (p.Ser57=) rs1555932401
NM_007194.4(CHEK2):c.189A>G (p.Leu63=) rs761028062
NM_007194.4(CHEK2):c.18T>C (p.Asp6=) rs1555932937
NM_007194.4(CHEK2):c.213C>G (p.Leu71=) rs1057524667
NM_007194.4(CHEK2):c.225T>G (p.Pro75=) rs1217608176
NM_007194.4(CHEK2):c.231_245CCAAGAACCTGAGGA[1] (p.77_81DQEPE[1]) rs587780181
NM_007194.4(CHEK2):c.240T>G (p.Pro80=) rs878854918
NM_007194.4(CHEK2):c.243G>A (p.Glu81=) rs1060504690
NM_007194.4(CHEK2):c.255T>C (p.Pro85=) rs1418971926
NM_007194.4(CHEK2):c.288A>G (p.Leu96=) rs767758092
NM_007194.4(CHEK2):c.319+17T>C rs770423802
NM_007194.4(CHEK2):c.319+3865T>C rs964218389
NM_007194.4(CHEK2):c.319+6A>G rs1555931991
NM_007194.4(CHEK2):c.319+7C>T rs1057522753
NM_007194.4(CHEK2):c.319+8C>G rs776443322
NM_007194.4(CHEK2):c.320-16T>C rs773890954
NM_007194.4(CHEK2):c.320-5T>A rs121908700
NM_007194.4(CHEK2):c.381A>G (p.Glu127=) rs199929178
NM_007194.4(CHEK2):c.384A>G (p.Pro128=) rs766409666
NM_007194.4(CHEK2):c.410G>A (p.Arg137Gln) rs368570187
NM_007194.4(CHEK2):c.417C>T (p.Tyr139=) rs200917541
NM_007194.4(CHEK2):c.432T>C (p.Phe144=) rs876658374
NM_007194.4(CHEK2):c.433C>A (p.Arg145=) rs137853007
NM_007194.4(CHEK2):c.444+19T>C rs200501745
NM_007194.4(CHEK2):c.444+20G>T rs755989738
NM_007194.4(CHEK2):c.445-10T>C rs1060504692
NM_007194.4(CHEK2):c.468C>T (p.Tyr156=) rs1555926996
NM_007194.4(CHEK2):c.471T>C (p.Ile157=) rs374170772
NM_007194.4(CHEK2):c.474A>C (p.Ala158=) rs745699485
NM_007194.4(CHEK2):c.474A>G (p.Ala158=) rs745699485
NM_007194.4(CHEK2):c.528G>C (p.Gly176=) rs587780889
NM_007194.4(CHEK2):c.539G>A (p.Arg180His) rs137853009
NM_007194.4(CHEK2):c.570A>T (p.Ala190=) rs754689169
NM_007194.4(CHEK2):c.573G>C (p.Leu191=) rs786201267
NM_007194.4(CHEK2):c.580A>T (p.Ser194Cys) rs786203042
NM_007194.4(CHEK2):c.592+11T>G rs1555926700
NM_007194.4(CHEK2):c.592+12_592+13del rs1555926694
NM_007194.4(CHEK2):c.592+16T>G rs1555926688
NM_007194.4(CHEK2):c.592+19G>T rs1569157121
NM_007194.4(CHEK2):c.592+5TAT[2] rs1555926697
NM_007194.4(CHEK2):c.592+9A>G rs538351542
NM_007194.4(CHEK2):c.593-11_593-7del rs863224414
NM_007194.4(CHEK2):c.593-15T>A rs757717459
NM_007194.4(CHEK2):c.593-18T>C rs1569150284
NM_007194.4(CHEK2):c.593-20T>G rs1555924584
NM_007194.4(CHEK2):c.593-20_593-18del rs752590759
NM_007194.4(CHEK2):c.593-7T>A rs1555924549
NM_007194.4(CHEK2):c.600C>G (p.Val200=) rs141685349
NM_007194.4(CHEK2):c.633T>C (p.Val211=) rs1555924460
NM_007194.4(CHEK2):c.642G>A (p.Lys214=) rs1569149867
NM_007194.4(CHEK2):c.645A>G (p.Ala215=) rs761630560
NM_007194.4(CHEK2):c.651A>G (p.Arg217=) rs774245273
NM_007194.4(CHEK2):c.654T>C (p.Asp218=) rs907621837
NM_007194.4(CHEK2):c.683+10T>C rs747427230
NM_007194.4(CHEK2):c.683+15T>G rs1569149564
NM_007194.4(CHEK2):c.683+9T>C rs1060504691
NM_007194.4(CHEK2):c.684-14G>C rs1555921411
NM_007194.4(CHEK2):c.684-16T>C rs1056041546
NM_007194.4(CHEK2):c.684-20A>G rs1057520266
NM_007194.4(CHEK2):c.684-3T>C rs1555921387
NM_007194.4(CHEK2):c.690C>G (p.Ala230=) rs1569140952
NM_007194.4(CHEK2):c.6T>C (p.Ser2=) rs768632104
NM_007194.4(CHEK2):c.705G>A (p.Lys235=) rs1555921297
NM_007194.4(CHEK2):c.714C>T (p.Phe238=) rs864622322
NM_007194.4(CHEK2):c.72C>T (p.Ser24=) rs759679862
NM_007194.4(CHEK2):c.738A>T (p.Val246=) rs1555921163
NM_007194.4(CHEK2):c.74T>C (p.Val25Ala) rs587780188
NM_007194.4(CHEK2):c.755G>A (p.Ser252Asn) rs587781379
NM_007194.4(CHEK2):c.765G>A (p.Lys255=) rs750596640
NM_007194.4(CHEK2):c.777T>C (p.Gly259=) rs876659828
NM_007194.4(CHEK2):c.792+11A>G rs765935437
NM_007194.4(CHEK2):c.793-11G>A rs5997387
NM_007194.4(CHEK2):c.793-12T>C rs1555920271
NM_007194.4(CHEK2):c.793-13C>T rs1555920274
NM_007194.4(CHEK2):c.793-17T>C rs778511901
NM_007194.4(CHEK2):c.846+15_846+16del rs775989721
NM_007194.4(CHEK2):c.846+6TAT[2] rs1555920076
NM_007194.4(CHEK2):c.847-15_847-14insGG rs1555917068
NM_007194.4(CHEK2):c.847-17T>C rs199780411
NM_007194.4(CHEK2):c.847-30_847-11dup rs760398606
NM_007194.4(CHEK2):c.847-33_847-14del rs1569128594
NM_007194.4(CHEK2):c.907T>C (p.Leu303=) rs752359705
NM_007194.4(CHEK2):c.908+10A>G rs774973319
NM_007194.4(CHEK2):c.908+11A>T rs1555916864
NM_007194.4(CHEK2):c.908+14T>G rs538313507
NM_007194.4(CHEK2):c.908+18T>A rs755416802
NM_007194.4(CHEK2):c.908+18del rs778668907
NM_007194.4(CHEK2):c.908+19A>T rs759973493
NM_007194.4(CHEK2):c.909-28_909-20del rs1555915597
NM_007194.4(CHEK2):c.918G>C (p.Gly306=) rs1057523756
NM_007194.4(CHEK2):c.942G>T (p.Val314=) rs1057520467
NM_007194.4(CHEK2):c.996C>T (p.Leu332=) rs1053994833
NM_007194.4(CHEK2):c.997T>C (p.Leu333=) rs1352758126

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