ClinVar Miner

List of variants in gene CHEK2 reported as likely benign for Familial cancer of breast

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 144
Download table as spreadsheet
HGVS dbSNP
NM_007194.3(CHEK2):c.444+10_444+13delGAAT rs1555927105
NM_007194.3(CHEK2):c.793-9_793-8delTT rs1480956379
NM_007194.3(CHEK2):c.847-10delC rs1060504694
NM_007194.4(CHEK2):c.1008+13C>T rs193264230
NM_007194.4(CHEK2):c.1008+8A>G rs139986197
NM_007194.4(CHEK2):c.1023C>T (p.Asn341=) rs377668478
NM_007194.4(CHEK2):c.102G>A (p.Gln34=) rs1555932675
NM_007194.4(CHEK2):c.1035C>T (p.His345=) rs756520206
NM_007194.4(CHEK2):c.1038T>C (p.Arg346=) rs1555914324
NM_007194.4(CHEK2):c.1050A>G (p.Pro350=) rs1555914312
NM_007194.4(CHEK2):c.1063C>T (p.Leu355=) rs786201130
NM_007194.4(CHEK2):c.1065G>A (p.Leu355=) rs938389349
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.1096-4T>C rs587782840
NM_007194.4(CHEK2):c.1113C>T (p.His371=) rs876659094
NM_007194.4(CHEK2):c.1149C>T (p.Thr383=) rs1555913842
NM_007194.4(CHEK2):c.1152A>G (p.Leu384=) rs1060502715
NM_007194.4(CHEK2):c.1164C>T (p.Pro388=) rs878854911
NM_007194.4(CHEK2):c.1167C>A (p.Thr389=) rs1314236188
NM_007194.4(CHEK2):c.1197T>C (p.Val399=) rs1057520268
NM_007194.4(CHEK2):c.1200G>C (p.Gly400=) rs876659590
NM_007194.4(CHEK2):c.1217G>A (p.Arg406His) rs200649225
NM_007194.4(CHEK2):c.1260-10C>G rs730881706
NM_007194.4(CHEK2):c.1260-6del rs878854912
NM_007194.4(CHEK2):c.1269G>T (p.Gly423=) rs749368980
NM_007194.4(CHEK2):c.1278T>G (p.Pro426=) rs1060504689
NM_007194.4(CHEK2):c.1287G>A (p.Glu429=) rs758102180
NM_007194.4(CHEK2):c.129C>A (p.Thr43=) rs786202779
NM_007194.4(CHEK2):c.129C>G (p.Thr43=) rs786202779
NM_007194.4(CHEK2):c.1302G>A (p.Val434=) rs1060504693
NM_007194.4(CHEK2):c.1312G>T (p.Asp438Tyr) rs200050883
NM_007194.4(CHEK2):c.1320C>T (p.Ile440=) rs1555913469
NM_007194.4(CHEK2):c.1323C>T (p.Thr441=) rs753839004
NM_007194.4(CHEK2):c.135G>A (p.Thr45=) rs745423387
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+10G>A rs1060504696
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>A (p.Leu499=) rs587780890
NM_007194.4(CHEK2):c.1497G>C (p.Leu499=) rs587780890
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.1506A>G (p.Glu502=) rs1555912021
NM_007194.4(CHEK2):c.1518A>G (p.Thr506=) rs1052262892
NM_007194.4(CHEK2):c.1543-10T>G rs1555911654
NM_007194.4(CHEK2):c.1557A>C (p.Arg519=) rs1555911615
NM_007194.4(CHEK2):c.1563G>A (p.Arg521=) rs761278013
NM_007194.4(CHEK2):c.156C>T (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.1597A>G (p.Thr533Ala) rs562517792
NM_007194.4(CHEK2):c.15G>A (p.Ser5=) rs145183886
NM_007194.4(CHEK2):c.1604G>A (p.Arg535His) rs544216926
NM_007194.4(CHEK2):c.1614G>A (p.Val538=) rs750337711
NM_007194.4(CHEK2):c.1620T>C (p.Ala540=) rs1194893297
NM_007194.4(CHEK2):c.1623T>C (p.Ala541=) rs773670297
NM_007194.4(CHEK2):c.1623T>G (p.Ala541=) rs773670297
NM_007194.4(CHEK2):c.177A>T (p.Thr59=) rs750143255
NM_007194.4(CHEK2):c.186C>T (p.Ser62=) rs786203025
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.254C>T (p.Pro85Leu) rs17883862
NM_007194.4(CHEK2):c.286T>C (p.Leu96=) rs1555932127
NM_007194.4(CHEK2):c.288A>G (p.Leu96=) rs767758092
NM_007194.4(CHEK2):c.294C>T (p.Ala98=) rs1555932111
NM_007194.4(CHEK2):c.319+7C>G rs1057522753
NM_007194.4(CHEK2):c.319+7C>T rs1057522753
NM_007194.4(CHEK2):c.319+8C>G rs776443322
NM_007194.4(CHEK2):c.320-5T>A rs121908700
NM_007194.4(CHEK2):c.320-7A>G rs1555927424
NM_007194.4(CHEK2):c.339C>T (p.Tyr113=) rs905674348
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.388C>T (p.Leu130=) rs1057522274
NM_007194.4(CHEK2):c.410G>A (p.Arg137Gln) rs368570187
NM_007194.4(CHEK2):c.411A>C (p.Arg137=) rs1060504695
NM_007194.4(CHEK2):c.414A>C (p.Thr138=) rs876658162
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.444+19T>C rs200501745
NM_007194.4(CHEK2):c.444+7_444+8insTCTCCTAG rs1555927106
NM_007194.4(CHEK2):c.445-10T>C rs1060504692
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.480A>G (p.Ile160Met) rs575910805
NM_007194.4(CHEK2):c.528G>C (p.Gly176=) rs587780889
NM_007194.4(CHEK2):c.534A>G (p.Gly178=) rs554465930
NM_007194.4(CHEK2):c.538C>T (p.Arg180Cys) rs77130927
NM_007194.4(CHEK2):c.555C>T (p.Asn185=) rs780782542
NM_007194.4(CHEK2):c.573G>C (p.Leu191=) rs786201267
NM_007194.4(CHEK2):c.582C>T (p.Ser194=) rs761126328
NM_007194.4(CHEK2):c.592+9A>G rs538351542
NM_007194.4(CHEK2):c.593-11_593-7del rs863224414
NM_007194.4(CHEK2):c.593-14C>G rs145754558
NM_007194.4(CHEK2):c.593-15T>A rs757717459
NM_007194.4(CHEK2):c.593-9C>T rs1057517597
NM_007194.4(CHEK2):c.600C>G (p.Val200=) rs141685349
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.683+10T>A rs747427230
NM_007194.4(CHEK2):c.683+10T>C rs747427230
NM_007194.4(CHEK2):c.683+9T>C rs1060504691
NM_007194.4(CHEK2):c.684-4C>G rs121908695
NM_007194.4(CHEK2):c.684-4C>T rs121908695
NM_007194.4(CHEK2):c.684-6C>T rs776400765
NM_007194.4(CHEK2):c.684-8C>T rs1555921406
NM_007194.4(CHEK2):c.6T>C (p.Ser2=) rs768632104
NM_007194.4(CHEK2):c.714C>T (p.Phe238=) rs864622322
NM_007194.4(CHEK2):c.717G>A (p.Glu239=) rs1555921253
NM_007194.4(CHEK2):c.72C>T (p.Ser24=) rs759679862
NM_007194.4(CHEK2):c.75T>C (p.Val25=) rs1555932812
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.78C>T (p.Thr26=) rs876658717
NM_007194.4(CHEK2):c.793-11G>A rs5997387
NM_007194.4(CHEK2):c.793-17T>C rs778511901
NM_007194.4(CHEK2):c.793-4A>G rs1212612057
NM_007194.4(CHEK2):c.846+10A>T rs1345067762
NM_007194.4(CHEK2):c.846+7A>G rs763340730
NM_007194.4(CHEK2):c.847-10C>G rs745745105
NM_007194.4(CHEK2):c.847-17T>C rs199780411
NM_007194.4(CHEK2):c.84C>A (p.Ser28=) rs863224415
NM_007194.4(CHEK2):c.84C>T (p.Ser28=) rs863224415
NM_007194.4(CHEK2):c.885A>G (p.Glu295=) rs1555916935
NM_007194.4(CHEK2):c.908+10A>G rs774973319
NM_007194.4(CHEK2):c.908+18T>A rs755416802
NM_007194.4(CHEK2):c.908+8G>A rs1555916871
NM_007194.4(CHEK2):c.909-10T>G rs864622231
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.925C>T (p.Leu309=) rs786202521
NM_007194.4(CHEK2):c.939G>A (p.Val313=) rs1555915485
NM_007194.4(CHEK2):c.955C>T (p.Leu319=) rs1057524600
NM_007194.4(CHEK2):c.997T>C (p.Leu333=) rs1352758126
NM_007194.4(CHEK2):c.99A>G (p.Ser33=) rs925489951

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.