ClinVar Miner

List of variants in gene KRAS reported as likely benign

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 133
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_033360.4(KRAS):c.*1759A>G rs4597149 0.99474
NM_033360.4(KRAS):c.*3907A>G rs8720 0.48208
NM_033360.4(KRAS):c.*633T>C rs9266 0.48177
NM_033360.4(KRAS):c.*3498C>T rs1137188 0.48161
NM_033360.4(KRAS):c.*4022A>C rs12587 0.48152
NM_033360.4(KRAS):c.*4200T>A rs12245 0.48134
NM_033360.4(KRAS):c.*3522T>A rs1137189 0.48000
NM_033360.4(KRAS):c.*3009A>G rs13096 0.45974
NM_033360.4(KRAS):c.*298T>G rs712 0.45514
NM_033360.4(KRAS):c.*3881A>C rs1137196 0.36455
NM_004985.5(KRAS):c.519T>C (p.Asp173=) rs1137282 0.19563
NM_033360.4(KRAS):c.*1708T>C rs7973450 0.19546
NM_033360.4(KRAS):c.*1204A>G rs7960917 0.18298
NM_033360.4(KRAS):c.*1776C>T rs7973623 0.18240
NM_004985.5(KRAS):c.451-9G>A rs12313763 0.08467
NM_033360.4(KRAS):c.*2626T>G rs61764370 0.06273
NM_033360.4(KRAS):c.*1094G>T rs61763590 0.06270
NM_033360.4(KRAS):c.*2305A>G rs61764368 0.04337
NM_004985.5(KRAS):c.450+304T>A rs1252899211 0.04067
NM_033360.4(KRAS):c.*4432A>G rs61764374 0.03798
NM_033360.4(KRAS):c.*3623T>A rs61764372 0.02189
NM_033360.4(KRAS):c.*1886T>C rs115968671 0.01694
NM_033360.4(KRAS):c.*3273G>A rs61764371 0.01646
NM_033360.4(KRAS):c.*945T>C rs61763589 0.01587
NM_033360.4(KRAS):c.5-240G>A rs61763587 0.01417
NM_004985.5(KRAS):c.450+296T>A rs1362019931 0.01277
NM_004985.5(KRAS):c.-12+116G>T rs61759619 0.01168
NM_033360.4(KRAS):c.*1183G>A rs61763591 0.00998
NM_033360.4(KRAS):c.291-311A>G rs138809689 0.00663
NM_033360.4(KRAS):c.*525T>C rs140080026 0.00652
NM_033360.4(KRAS):c.*1758_*1759del rs535478558 0.00456
NM_033360.4(KRAS):c.451-224T>A rs145862422 0.00456
NM_033360.4(KRAS):c.*1661T>C rs61764366 0.00455
NM_033360.4(KRAS):c.*2492C>T rs61764369 0.00439
NM_004985.5(KRAS):c.291-128T>G rs113376636 0.00419
NM_004985.5(KRAS):c.-11-324T>G rs61759634 0.00399
NM_033360.4(KRAS):c.111+239A>G rs187904655 0.00386
NM_033360.4(KRAS):c.111+46T>G rs199716819 0.00143
NM_033360.4(KRAS):c.*3766A>G rs529959450 0.00108
NM_033360.4(KRAS):c.5-18A>G rs200189105 0.00100
NM_033360.4(KRAS):c.*1826C>G rs539213224 0.00073
NM_004985.5(KRAS):c.451-5565G>A rs200970347 0.00031
NM_004985.5(KRAS):c.24A>G (p.Val8=) rs147406419 0.00025
NM_004985.5(KRAS):c.264A>G (p.Lys88=) rs370920665 0.00021
NM_033360.4(KRAS):c.*4549G>C rs545014897 0.00020
NM_004985.5(KRAS):c.451-5535A>C rs201170656 0.00019
NM_004985.5(KRAS):c.198A>G (p.Ala66=) rs200229810 0.00016
NM_004985.5(KRAS):c.451-14T>C rs372508498 0.00014
NM_033360.4(KRAS):c.90C>T (p.Asp30=) rs113623140 0.00011
NM_033360.4(KRAS):c.5-11A>G rs369047577 0.00008
NM_004985.5(KRAS):c.451-5560T>A rs373169526 0.00006
NM_033360.4(KRAS):c.4+5G>A rs201789109 0.00006
NM_004985.5(KRAS):c.451-5652C>T rs727505314 0.00004
NM_033360.4(KRAS):c.112-10C>T rs760989619 0.00004
NM_033360.4(KRAS):c.93A>G (p.Glu31=) rs377354475 0.00004
NM_004985.5(KRAS):c.112-14T>G rs1374246336 0.00003
NM_004985.5(KRAS):c.451-5604T>A rs397517476 0.00002
NM_033360.4(KRAS):c.*103A>G rs1213931592 0.00002
NM_033360.4(KRAS):c.*16T>C rs779184057 0.00002
NM_033360.4(KRAS):c.249C>T (p.Ala83=) rs751117590 0.00002
NM_004985.5(KRAS):c.111+8T>G rs779370636 0.00001
NM_004985.5(KRAS):c.112-12C>T rs202104024 0.00001
NM_004985.5(KRAS):c.15A>G (p.Lys5=) rs104894361 0.00001
NM_004985.5(KRAS):c.171C>T (p.Asp57=) rs1951406780 0.00001
NM_004985.5(KRAS):c.291-18C>T rs995378646 0.00001
NM_004985.5(KRAS):c.411T>C (p.Tyr137=) rs752731198 0.00001
NM_004985.5(KRAS):c.451-5542C>T rs201967696 0.00001
NM_004985.5(KRAS):c.456T>G (p.Val152=) rs767947451 0.00001
NM_004985.5(KRAS):c.60G>A (p.Thr20=) rs747140926 0.00001
NM_033360.4(KRAS):c.-9C>T rs370230526 0.00001
NM_033360.4(KRAS):c.112-5C>T rs376520586 0.00001
NM_033360.4(KRAS):c.417T>C (p.Ile139=) rs1555193843 0.00001
NM_033360.4(KRAS):c.450+13G>A rs1057523949 0.00001
NM_004985.5(KRAS):c.*4059A>G
NM_004985.5(KRAS):c.105A>C (p.Thr35=)
NM_004985.5(KRAS):c.111+10G>A
NM_004985.5(KRAS):c.111+16A>G
NM_004985.5(KRAS):c.112-12C>G
NM_004985.5(KRAS):c.112-20C>A
NM_004985.5(KRAS):c.112-9C>T rs727504298
NM_004985.5(KRAS):c.120C>T (p.Tyr40=)
NM_004985.5(KRAS):c.132A>G (p.Val44=)
NM_004985.5(KRAS):c.141T>C (p.Asp47=)
NM_004985.5(KRAS):c.156C>T (p.Leu52=)
NM_004985.5(KRAS):c.168C>T (p.Leu56=)
NM_004985.5(KRAS):c.186G>A (p.Glu62=) rs1407455199
NM_004985.5(KRAS):c.261T>G (p.Thr87=)
NM_004985.5(KRAS):c.290+11A>G
NM_004985.5(KRAS):c.290+18A>G rs1951404839
NM_004985.5(KRAS):c.290+7T>A
NM_004985.5(KRAS):c.291-10del rs727503991
NM_004985.5(KRAS):c.291-6del rs1225182964
NM_004985.5(KRAS):c.33T>C (p.Ala11=) rs397517039
NM_004985.5(KRAS):c.348T>C (p.Asn116=)
NM_004985.5(KRAS):c.358T>C (p.Leu120=)
NM_004985.5(KRAS):c.36T>A (p.Gly12=)
NM_004985.5(KRAS):c.36T>G (p.Gly12=)
NM_004985.5(KRAS):c.372A>G (p.Thr124=) rs2141506083
NM_004985.5(KRAS):c.375A>G (p.Val125=)
NM_004985.5(KRAS):c.426T>A (p.Ile142=)
NM_004985.5(KRAS):c.432A>G (p.Thr144=)
NM_004985.5(KRAS):c.435A>T (p.Ser145=)
NM_004985.5(KRAS):c.438A>G (p.Ala146=)
NM_004985.5(KRAS):c.450+11C>G rs727504633
NM_004985.5(KRAS):c.451-10T>C rs876657481
NM_004985.5(KRAS):c.451-12T>G
NM_004985.5(KRAS):c.451-5327G>A rs114748473
NM_004985.5(KRAS):c.451-5575A>G rs1555192913
NM_004985.5(KRAS):c.451-5604T>C rs397517476
NM_004985.5(KRAS):c.453T>C (p.Gly151=) rs2141481751
NM_004985.5(KRAS):c.465C>G (p.Ala155=)
NM_004985.5(KRAS):c.474A>G (p.Thr158=)
NM_004985.5(KRAS):c.481C>A (p.Arg161=) rs1951184515
NM_004985.5(KRAS):c.498T>C (p.His166=)
NM_004985.5(KRAS):c.507G>A (p.Lys169=)
NM_004985.5(KRAS):c.528GAA[1] (p.Lys180del) rs397517043
NM_004985.5(KRAS):c.535AAG[1] (p.Lys180del) rs749587181
NM_004985.5(KRAS):c.54C>T (p.Ala18=)
NM_004985.5(KRAS):c.66G>A (p.Gln22=)
NM_004985.5(KRAS):c.69A>G (p.Leu23=)
NM_033360.4(KRAS):c.*134C>T rs1057522250
NM_033360.4(KRAS):c.*1539_*1541del rs200038818
NM_033360.4(KRAS):c.*1748dup rs71065923
NM_033360.4(KRAS):c.*2400dup rs56128001
NM_033360.4(KRAS):c.*3385del rs34176876
NM_033360.4(KRAS):c.*3804dup rs142323886
NM_033360.4(KRAS):c.*4186_*4187del rs34719539
NM_033360.4(KRAS):c.*4426_*4427dup rs61764373
NM_033360.4(KRAS):c.*44C>T rs1555192443
NM_033360.4(KRAS):c.*671C>T rs566222739
NM_033360.4(KRAS):c.255T>C (p.Asn85=) rs1592808282
NM_033360.4(KRAS):c.450+16A>G rs1555193834
NM_033360.4(KRAS):c.500G>C (p.Arg167Thr)

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.