Primary Site >> Stomach Cancer

Gene >> ARID2

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000334344
Start 45850730:45850730(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2607T>G
AA Mutation p.Asn869Lys(p.N869K)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000334344
Start 45817864:45817864(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.613G>A
AA Mutation p.Ala205Thr(p.A205T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000334344
Start 45817871:45817871(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.620C>T
AA Mutation p.Ala207Val(p.A207V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000334344
Start 45836599:45836599(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.716A>T
AA Mutation p.Asp239Val(p.D239V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000334344
Start 45836896:45836896(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.928C>T
AA Mutation p.Arg310Cys(p.R310C)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000334344
Start 45852451:45852451(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.4328G>A
AA Mutation p.Ser1443Asn(p.S1443N)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 7
Mutation Consequence missense_variant
Transcription ID ENST00000334344
Start 45852513:45852513(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs760589011
CDS Mutation c.4390C>T
AA Mutation p.Arg1464Cys(p.R1464C)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 8
Mutation Consequence missense_variant
Transcription ID ENST00000334344
Start 45893488:45893488(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.5216C>G
AA Mutation p.Ala1739Gly(p.A1739G)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 9
Mutation Consequence missense_variant
Transcription ID ENST00000334344
Start 45836822:45836822(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.854G>A
AA Mutation p.Arg285Gln(p.R285Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 10
Mutation Consequence missense_variant
Transcription ID ENST00000334344
Start 45852619:45852619(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.4496T>C
AA Mutation p.Leu1499Pro(p.L1499P)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 11
Mutation Consequence missense_variant
Transcription ID ENST00000334344
Start 45730112:45730112(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.161T>C
AA Mutation p.Val54Ala(p.V54A)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 12
Mutation Consequence missense_variant
Transcription ID ENST00000334344
Start 45891856:45891856(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.4999T>C
AA Mutation p.Cys1667Arg(p.C1667R)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 13
Mutation Consequence missense_variant
Transcription ID ENST00000334344
Start 45837527:45837527(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1150G>C
AA Mutation p.Ala384Pro(p.A384P)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 14
Mutation Consequence missense_variant
Transcription ID ENST00000334344
Start 45852514:45852514(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs770601353
CDS Mutation c.4391G>A
AA Mutation p.Arg1464His(p.R1464H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 15
Mutation Consequence missense_variant
Transcription ID ENST00000334344
Start 45817786:45817786(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.535G>A
AA Mutation p.Val179Ile(p.V179I)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 16
Mutation Consequence missense_variant
Transcription ID ENST00000334344
Start 45836622:45836622(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.739C>T
AA Mutation p.Arg247Cys(p.R247C)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 17
Mutation Consequence missense_variant
Transcription ID ENST00000334344
Start 45817735:45817735(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.484G>T
AA Mutation p.Val162Leu(p.V162L)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 18
Mutation Consequence missense_variant
Transcription ID ENST00000334344
Start 45836604:45836604(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs186180564
CDS Mutation c.721G>A
AA Mutation p.Val241Ile(p.V241I)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 19
Mutation Consequence missense_variant
Transcription ID ENST00000334344
Start 45846904:45846904(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1547T>C
AA Mutation p.Val516Ala(p.V516A)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 20
Mutation Consequence synonymous_variant
Transcription ID ENST00000334344
Start 45850772:45850772(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2649C>G
Mutation Classification Silent
Feature Type Transcript
ID 21
Mutation Consequence synonymous_variant
Transcription ID ENST00000334344
Start 45852767:45852767(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.4644C>A
Mutation Classification Silent
Feature Type Transcript
ID 22
Mutation Consequence synonymous_variant
Transcription ID ENST00000334344
Start 45851561:45851561(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs202093863
CDS Mutation c.3438G>A
Mutation Classification Silent
Feature Type Transcript
ID 23
Mutation Consequence synonymous_variant
Transcription ID ENST00000334344
Start 45821481:45821481(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs778247043
CDS Mutation c.699C>T
Mutation Classification Silent
Feature Type Transcript
ID 24
Mutation Consequence synonymous_variant
Transcription ID ENST00000334344
Start 45852266:45852266(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs146664069
CDS Mutation c.4143T>G
Mutation Classification Silent
Feature Type Transcript
ID 25
Mutation Consequence frameshift_variant
Transcription ID ENST00000334344
Start 45851184:45851184(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.3065delC
AA Mutation p.Pro1022HisfsTer38(p.P1022Hfs*38)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 26
Mutation Consequence frameshift_variant
Transcription ID ENST00000334344
Start 45904940:45904941(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.5371_5372delAA
AA Mutation p.Lys1791GlufsTer3(p.K1791Efs*3)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 27
Mutation Consequence frameshift_variant
Transcription ID ENST00000334344
Start 45850120:45850120(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.1999delA
AA Mutation p.Met667CysfsTer34(p.M667Cfs*34)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 28
Mutation Consequence frameshift_variant
Transcription ID ENST00000334344
Start 45852742:45852745(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.4621_4624delATCA
AA Mutation p.Ile1541ValfsTer24(p.I1541Vfs*24)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 29
Mutation Consequence frameshift_variant
Transcription ID ENST00000334344
Start 45811452:45811452(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.322delG
AA Mutation p.Glu108ArgfsTer107(p.E108Rfs*107)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 30
Mutation Consequence frameshift_variant
Transcription ID ENST00000334344
Start 45860909:45860909(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.4883delC
AA Mutation p.Pro1628LeufsTer73(p.P1628Lfs*73)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 31
Mutation Consequence frameshift_variant
Transcription ID ENST00000334344
Start 45851535:45851535(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.3416delG
AA Mutation p.Gly1139GlufsTer17(p.G1139Efs*17)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 32
Mutation Consequence frameshift_variant
Transcription ID ENST00000334344
Start 45821431:45821431(version: GRCh38)
Mutation Type DEL
dbSNP_RS null
CDS Mutation c.652delT
AA Mutation p.Ser218ProfsTer74(p.S218Pfs*74)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 33
Mutation Consequence frameshift_variant
Transcription ID ENST00000334344
Start 45851666:45851666(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.3546delT
AA Mutation p.Phe1182LeufsTer6(p.F1182Lfs*6)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 34
Mutation Consequence stop_gained
Transcription ID ENST00000334344
Start 45851244:45851244(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3121C>T
AA Mutation p.Gln1041Ter(p.Q1041*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript
ID 35
Mutation Consequence stop_gained;frameshift_variant
Transcription ID ENST00000334344
Start 45850731:45850732(version: GRCh38)
Mutation Type INS
dbSNP_RS novel
CDS Mutation c.2608_2609insACTGAAC
AA Mutation p.Phe870TyrfsTer2(p.F870Yfs*2)
Mutation Classification Nonsense_Mutation
Feature Type Transcript
ID 36
Mutation Consequence stop_gained
Transcription ID ENST00000334344
Start 45851409:45851409(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3286C>T
AA Mutation p.Gln1096Ter(p.Q1096*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript
ID 37
Mutation Consequence stop_gained
Transcription ID ENST00000334344
Start 45850572:45850572(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2449C>T
AA Mutation p.Gln817Ter(p.Q817*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript
ID 38
Mutation Consequence stop_gained
Transcription ID ENST00000334344
Start 45852567:45852567(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.4444C>T
AA Mutation p.Gln1482Ter(p.Q1482*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript
ID 39
Mutation Consequence stop_gained
Transcription ID ENST00000334344
Start 45837566:45837566(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1189C>T
AA Mutation p.Gln397Ter(p.Q397*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript
ID 40
Mutation Consequence stop_gained
Transcription ID ENST00000334344
Start 45851937:45851937(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3814C>T
AA Mutation p.Arg1272Ter(p.R1272*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript
ID 41
Mutation Consequence stop_gained
Transcription ID ENST00000334344
Start 45849635:45849635(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1771C>T
AA Mutation p.Gln591Ter(p.Q591*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript
ID 42
Mutation Consequence frameshift_variant
Transcription ID ENST00000334344
Start 45850208:45850209(version: GRCh38)
Mutation Type INS
dbSNP_RS novel
CDS Mutation c.2086dupC
AA Mutation p.Gln696ProfsTer11(p.Q696Pfs*11)
Mutation Classification Frame_Shift_Ins
Feature Type Transcript
ID 43
Mutation Consequence splice_acceptor_variant
Transcription ID ENST00000334344
Start 45904933:45904933(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.5364-1G>C
Mutation Classification Splice_Site
Feature Type Transcript
ID 44
Mutation Consequence splice_donor_variant;coding_sequence_variant;intron_variant
Transcription ID ENST00000334344
Start 45846936:45846955(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.1580_1580+19delGGTAAGTGGTTTATTTCTAT
Mutation Classification Splice_Site
Feature Type Transcript
ID 45
Mutation Consequence splice_acceptor_variant
Transcription ID ENST00000334344
Start 45893629:45893629(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.5272-1G>T
Mutation Classification Splice_Site
Feature Type Transcript