Primary Site >> Stomach Cancer

Gene >> KMT2B

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000420124
Start 35738094:35738094(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.7775A>G
AA Mutation p.Lys2592Arg(p.K2592R)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000420124
Start 35722682:35722682(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2686C>A
AA Mutation p.Leu896Ile(p.L896I)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000420124
Start 35725073:35725073(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3514C>T
AA Mutation p.Arg1172Cys(p.R1172C)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000420124
Start 35727518:35727518(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs747829749
CDS Mutation c.4198C>T
AA Mutation p.Arg1400Cys(p.R1400C)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000420124
Start 35719807:35719807(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs780868475
CDS Mutation c.460C>T
AA Mutation p.Arg154Cys(p.R154C)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000420124
Start 35737140:35737140(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.7427C>T
AA Mutation p.Ala2476Val(p.A2476V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 7
Mutation Consequence missense_variant
Transcription ID ENST00000420124
Start 35723181:35723181(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs780053167
CDS Mutation c.2909G>A
AA Mutation p.Arg970Gln(p.R970Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 8
Mutation Consequence missense_variant
Transcription ID ENST00000420124
Start 35738109:35738109(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.7790C>T
AA Mutation p.Ala2597Val(p.A2597V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 9
Mutation Consequence missense_variant
Transcription ID ENST00000420124
Start 35732575:35732575(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.6026C>T
AA Mutation p.Ala2009Val(p.A2009V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 10
Mutation Consequence missense_variant
Transcription ID ENST00000420124
Start 35733631:35733631(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs759167832
CDS Mutation c.6994C>T
AA Mutation p.Arg2332Cys(p.R2332C)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 11
Mutation Consequence missense_variant
Transcription ID ENST00000420124
Start 35738355:35738355(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.7946G>A
AA Mutation p.Arg2649His(p.R2649H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 12
Mutation Consequence missense_variant
Transcription ID ENST00000420124
Start 35732823:35732823(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.6274C>T
AA Mutation p.Arg2092Trp(p.R2092W)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 13
Mutation Consequence missense_variant
Transcription ID ENST00000420124
Start 35738127:35738127(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.7808A>C
AA Mutation p.Glu2603Ala(p.E2603A)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 14
Mutation Consequence missense_variant
Transcription ID ENST00000420124
Start 35730714:35730714(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.5284C>T
AA Mutation p.Arg1762Cys(p.R1762C)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 15
Mutation Consequence missense_variant
Transcription ID ENST00000420124
Start 35727495:35727495(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.4175C>A
AA Mutation p.Pro1392Gln(p.P1392Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 16
Mutation Consequence missense_variant
Transcription ID ENST00000420124
Start 35719802:35719802(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs746908334
CDS Mutation c.455G>A
AA Mutation p.Arg152Gln(p.R152Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 17
Mutation Consequence missense_variant
Transcription ID ENST00000420124
Start 35729005:35729005(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.4708G>A
AA Mutation p.Ala1570Thr(p.A1570T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 18
Mutation Consequence missense_variant
Transcription ID ENST00000420124
Start 35729283:35729283(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.4904G>T
AA Mutation p.Arg1635Leu(p.R1635L)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 19
Mutation Consequence missense_variant
Transcription ID ENST00000420124
Start 35719939:35719939(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.592C>T
AA Mutation p.Arg198Trp(p.R198W)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 20
Mutation Consequence missense_variant
Transcription ID ENST00000420124
Start 35738288:35738288(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.7879G>A
AA Mutation p.Gly2627Arg(p.G2627R)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 21
Mutation Consequence missense_variant
Transcription ID ENST00000420124
Start 35720950:35720950(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1603C>T
AA Mutation p.Arg535Cys(p.R535C)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 22
Mutation Consequence missense_variant
Transcription ID ENST00000420124
Start 35728128:35728128(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs748191051
CDS Mutation c.4528G>A
AA Mutation p.Ala1510Thr(p.A1510T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 23
Mutation Consequence missense_variant
Transcription ID ENST00000420124
Start 35720039:35720039(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.692G>A
AA Mutation p.Cys231Tyr(p.C231Y)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 24
Mutation Consequence missense_variant
Transcription ID ENST00000420124
Start 35722444:35722444(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs377636814
CDS Mutation c.2543C>T
AA Mutation p.Ser848Leu(p.S848L)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 25
Mutation Consequence missense_variant
Transcription ID ENST00000420124
Start 35730422:35730422(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.5157C>A
AA Mutation p.Phe1719Leu(p.F1719L)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 26
Mutation Consequence synonymous_variant
Transcription ID ENST00000420124
Start 35723029:35723029(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs767059945
CDS Mutation c.2757G>A
Mutation Classification Silent
Feature Type Transcript
ID 27
Mutation Consequence synonymous_variant
Transcription ID ENST00000420124
Start 35732531:35732531(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs763243718
CDS Mutation c.5982G>A
Mutation Classification Silent
Feature Type Transcript
ID 28
Mutation Consequence synonymous_variant
Transcription ID ENST00000420124
Start 35720307:35720307(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.960C>A
Mutation Classification Silent
Feature Type Transcript
ID 29
Mutation Consequence synonymous_variant
Transcription ID ENST00000420124
Start 35725288:35725288(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs780126664
CDS Mutation c.3597C>T
Mutation Classification Silent
Feature Type Transcript
ID 30
Mutation Consequence synonymous_variant
Transcription ID ENST00000420124
Start 35723176:35723176(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2904C>T
Mutation Classification Silent
Feature Type Transcript
ID 31
Mutation Consequence synonymous_variant
Transcription ID ENST00000420124
Start 35732375:35732375(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.5826C>A
Mutation Classification Silent
Feature Type Transcript
ID 32
Mutation Consequence synonymous_variant
Transcription ID ENST00000420124
Start 35737210:35737210(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.7497G>A
Mutation Classification Silent
Feature Type Transcript
ID 33
Mutation Consequence synonymous_variant
Transcription ID ENST00000420124
Start 35728115:35728115(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.4515C>T
Mutation Classification Silent
Feature Type Transcript
ID 34
Mutation Consequence synonymous_variant
Transcription ID ENST00000420124
Start 35738527:35738527(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs368314479
CDS Mutation c.8118C>T
Mutation Classification Silent
Feature Type Transcript
ID 35
Mutation Consequence synonymous_variant
Transcription ID ENST00000420124
Start 35723955:35723955(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3282C>T
Mutation Classification Silent
Feature Type Transcript
ID 36
Mutation Consequence synonymous_variant
Transcription ID ENST00000420124
Start 35721636:35721636(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs200332721
CDS Mutation c.2289G>A
Mutation Classification Silent
Feature Type Transcript
ID 37
Mutation Consequence synonymous_variant
Transcription ID ENST00000420124
Start 35730587:35730587(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.5247C>T
Mutation Classification Silent
Feature Type Transcript
ID 38
Mutation Consequence synonymous_variant
Transcription ID ENST00000420124
Start 35730395:35730395(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs372951507
CDS Mutation c.5130C>T
Mutation Classification Silent
Feature Type Transcript
ID 39
Mutation Consequence frameshift_variant
Transcription ID ENST00000420124
Start 35723813:35723813(version: GRCh38)
Mutation Type DEL
dbSNP_RS null
CDS Mutation c.3145delG
AA Mutation p.Ala1049ArgfsTer133(p.A1049Rfs*133)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 40
Mutation Consequence frameshift_variant
Transcription ID ENST00000420124
Start 35719862:35719862(version: GRCh38)
Mutation Type DEL
dbSNP_RS null
CDS Mutation c.521delC
AA Mutation p.Pro174GlnfsTer20(p.P174Qfs*20)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 41
Mutation Consequence frameshift_variant
Transcription ID ENST00000420124
Start 35725288:35725288(version: GRCh38)
Mutation Type DEL
dbSNP_RS null
CDS Mutation c.3602delC
AA Mutation p.Pro1201ArgfsTer154(p.P1201Rfs*154)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 42
Mutation Consequence frameshift_variant
Transcription ID ENST00000420124
Start 35738404:35738404(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.7995delC
AA Mutation p.His2665GlnfsTer73(p.H2665Qfs*73)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 43
Mutation Consequence frameshift_variant
Transcription ID ENST00000420124
Start 35732274:35732274(version: GRCh38)
Mutation Type DEL
dbSNP_RS null
CDS Mutation c.5730delC
AA Mutation p.Arg1911AspfsTer23(p.R1911Dfs*23)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 44
Mutation Consequence frameshift_variant
Transcription ID ENST00000420124
Start 35720997:35720997(version: GRCh38)
Mutation Type DEL
dbSNP_RS null
CDS Mutation c.1656delC
AA Mutation p.Lys553AsnfsTer52(p.K553Nfs*52)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 45
Mutation Consequence frameshift_variant
Transcription ID ENST00000420124
Start 35732101:35732101(version: GRCh38)
Mutation Type DEL
dbSNP_RS null
CDS Mutation c.5636delG
AA Mutation p.Gly1879ValfsTer16(p.G1879Vfs*16)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 46
Mutation Consequence frameshift_variant
Transcription ID ENST00000420124
Start 35723827:35723827(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.3159delG
AA Mutation p.Arg1055GlyfsTer127(p.R1055Gfs*127)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 47
Mutation Consequence frameshift_variant
Transcription ID ENST00000420124
Start 35727550:35727550(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.4235delG
AA Mutation p.Gly1412AlafsTer10(p.G1412Afs*10)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 48
Mutation Consequence frameshift_variant
Transcription ID ENST00000420124
Start 35720281:35720281(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.939delA
AA Mutation p.Val314Ter(p.V314*)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 49
Mutation Consequence frameshift_variant
Transcription ID ENST00000420124
Start 35733830:35733830(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.7121delC
AA Mutation p.Pro2374GlnfsTer65(p.P2374Qfs*65)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 50
Mutation Consequence frameshift_variant
Transcription ID ENST00000420124
Start 35723970:35723970(version: GRCh38)
Mutation Type DEL
dbSNP_RS null
CDS Mutation c.3302delC
AA Mutation p.Pro1101LeufsTer81(p.P1101Lfs*81)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 51
Mutation Consequence frameshift_variant
Transcription ID ENST00000420124
Start 35730787:35730787(version: GRCh38)
Mutation Type DEL
dbSNP_RS null
CDS Mutation c.5361delG
AA Mutation p.Pro1788ArgfsTer107(p.P1788Rfs*107)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 52
Mutation Consequence frameshift_variant
Transcription ID ENST00000420124
Start 35725283:35725283(version: GRCh38)
Mutation Type DEL
dbSNP_RS null
CDS Mutation c.3596delG
AA Mutation p.Gly1199AlafsTer156(p.G1199Afs*156)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 53
Mutation Consequence stop_gained
Transcription ID ENST00000420124
Start 35727522:35727522(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.4202G>A
AA Mutation p.Trp1401Ter(p.W1401*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript
ID 54
Mutation Consequence stop_gained
Transcription ID ENST00000420124
Start 35732060:35732060(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.5590C>T
AA Mutation p.Arg1864Ter(p.R1864*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript
ID 55
Mutation Consequence stop_gained
Transcription ID ENST00000420124
Start 35720980:35720980(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1633C>T
AA Mutation p.Arg545Ter(p.R545*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript
ID 56
Mutation Consequence frameshift_variant
Transcription ID ENST00000420124
Start 35723969:35723970(version: GRCh38)
Mutation Type INS
dbSNP_RS novel
CDS Mutation c.3302dupC
AA Mutation p.Ala1102CysfsTer11(p.A1102Cfs*11)
Mutation Classification Frame_Shift_Ins
Feature Type Transcript
ID 57
Mutation Consequence frameshift_variant
Transcription ID ENST00000420124
Start 35725287:35725288(version: GRCh38)
Mutation Type INS
dbSNP_RS novel
CDS Mutation c.3602dupC
AA Mutation p.Met1202AspfsTer22(p.M1202Dfs*22)
Mutation Classification Frame_Shift_Ins
Feature Type Transcript
ID 58
Mutation Consequence splice_acceptor_variant
Transcription ID ENST00000420124
Start 35724988:35724988(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3430-1G>T
Mutation Classification Splice_Site
Feature Type Transcript
ID 59
Mutation Consequence splice_donor_variant
Transcription ID ENST00000420124
Start 35727788:35727788(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.4392+1G>A
Mutation Classification Splice_Site
Feature Type Transcript
ID 60
Mutation Consequence inframe_deletion
Transcription ID ENST00000420124
Start 35738172:35738174(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.7855_7857delAAG
AA Mutation p.Lys2619del(p.K2619del)
Mutation Classification In_Frame_Del
Feature Type Transcript