Primary Site >> Stomach Cancer

Gene >> DST

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000312431
Start 56640592:56640592(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs543868808
CDS Mutation c.1528C>T
AA Mutation p.Arg510Cys(p.R510C)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000312431
Start 56628091:56628091(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.4033T>A
AA Mutation p.Trp1345Arg(p.W1345R)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000312431
Start 56460250:56460250(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs532258725
CDS Mutation c.16232C>T
AA Mutation p.Thr5411Met(p.T5411M)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000312431
Start 56552218:56552218(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs756527130
CDS Mutation c.9803C>T
AA Mutation p.Thr3268Met(p.T3268M)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000312431
Start 56552321:56552321(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs754589018
CDS Mutation c.9700A>G
AA Mutation p.Ile3234Val(p.I3234V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000312431
Start 56527665:56527665(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.10979T>G
AA Mutation p.Leu3660Arg(p.L3660R)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 7
Mutation Consequence missense_variant
Transcription ID ENST00000312431
Start 56555461:56555461(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.8249C>T
AA Mutation p.Ala2750Val(p.A2750V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 8
Mutation Consequence missense_variant
Transcription ID ENST00000312431
Start 56517601:56517601(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.11378C>T
AA Mutation p.Ala3793Val(p.A3793V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 9
Mutation Consequence missense_variant
Transcription ID ENST00000312431
Start 56498023:56498023(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.13156T>A
AA Mutation p.Ser4386Thr(p.S4386T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 10
Mutation Consequence missense_variant
Transcription ID ENST00000312431
Start 56509833:56509833(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.12050G>A
AA Mutation p.Arg4017His(p.R4017H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 11
Mutation Consequence missense_variant
Transcription ID ENST00000312431
Start 56511335:56511335(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.11871G>T
AA Mutation p.Gln3957His(p.Q3957H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 12
Mutation Consequence missense_variant
Transcription ID ENST00000312431
Start 56463666:56463666(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs776951210
CDS Mutation c.16015C>T
AA Mutation p.Arg5339Trp(p.R5339W)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 13
Mutation Consequence missense_variant
Transcription ID ENST00000312431
Start 56497860:56497860(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.13319G>A
AA Mutation p.Arg4440His(p.R4440H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 14
Mutation Consequence missense_variant
Transcription ID ENST00000312431
Start 56517230:56517230(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs375644963
CDS Mutation c.11554G>A
AA Mutation p.Ala3852Thr(p.A3852T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 15
Mutation Consequence missense_variant
Transcription ID ENST00000312431
Start 56489581:56489581(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.14015A>G
AA Mutation p.Glu4672Gly(p.E4672G)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 16
Mutation Consequence missense_variant
Transcription ID ENST00000312431
Start 56552369:56552369(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.9652A>G
AA Mutation p.Lys3218Glu(p.K3218E)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 17
Mutation Consequence missense_variant
Transcription ID ENST00000312431
Start 56497875:56497875(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.13304T>A
AA Mutation p.Leu4435Gln(p.L4435Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 18
Mutation Consequence missense_variant
Transcription ID ENST00000312431
Start 56526519:56526519(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.11200A>C
AA Mutation p.Asn3734His(p.N3734H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 19
Mutation Consequence missense_variant
Transcription ID ENST00000312431
Start 56517202:56517202(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.11582T>A
AA Mutation p.Met3861Lys(p.M3861K)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 20
Mutation Consequence missense_variant
Transcription ID ENST00000312431
Start 56670776:56670776(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.566A>G
AA Mutation p.Glu189Gly(p.E189G)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 21
Mutation Consequence missense_variant
Transcription ID ENST00000312431
Start 56642016:56642016(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs751086390
CDS Mutation c.1445G>A
AA Mutation p.Arg482His(p.R482H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 22
Mutation Consequence missense_variant
Transcription ID ENST00000312431
Start 56569883:56569883(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.7080T>G
AA Mutation p.Asp2360Glu(p.D2360E)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 23
Mutation Consequence missense_variant
Transcription ID ENST00000312431
Start 56573010:56573010(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.6520A>G
AA Mutation p.Lys2174Glu(p.K2174E)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 24
Mutation Consequence missense_variant
Transcription ID ENST00000312431
Start 56527632:56527632(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs764588106
CDS Mutation c.11012C>T
AA Mutation p.Ala3671Val(p.A3671V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 25
Mutation Consequence missense_variant
Transcription ID ENST00000312431
Start 56597822:56597822(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.5342A>G
AA Mutation p.Asn1781Ser(p.N1781S)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 26
Mutation Consequence missense_variant
Transcription ID ENST00000312431
Start 56630264:56630264(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.3749A>G
AA Mutation p.Asn1250Ser(p.N1250S)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 27
Mutation Consequence missense_variant
Transcription ID ENST00000312431
Start 56552194:56552194(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.9827A>C
AA Mutation p.Asn3276Thr(p.N3276T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 28
Mutation Consequence missense_variant
Transcription ID ENST00000312431
Start 56517226:56517226(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.11558G>A
AA Mutation p.Cys3853Tyr(p.C3853Y)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 29
Mutation Consequence missense_variant
Transcription ID ENST00000312431
Start 56625197:56625197(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs757972504
CDS Mutation c.4277G>A
AA Mutation p.Arg1426His(p.R1426H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 30
Mutation Consequence missense_variant
Transcription ID ENST00000312431
Start 56636568:56636568(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2536G>A
AA Mutation p.Ala846Thr(p.A846T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 31
Mutation Consequence missense_variant
Transcription ID ENST00000312431
Start 56572854:56572854(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.6676G>A
AA Mutation p.Glu2226Lys(p.E2226K)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 32
Mutation Consequence missense_variant
Transcription ID ENST00000312431
Start 56529579:56529579(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.10693A>T
AA Mutation p.Asn3565Tyr(p.N3565Y)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 33
Mutation Consequence missense_variant
Transcription ID ENST00000312431
Start 56466170:56466170(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs766884642
CDS Mutation c.15824T>C
AA Mutation p.Leu5275Pro(p.L5275P)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 34
Mutation Consequence missense_variant
Transcription ID ENST00000312431
Start 56593685:56593685(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.5933G>A
AA Mutation p.Arg1978Gln(p.R1978Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 35
Mutation Consequence missense_variant
Transcription ID ENST00000312431
Start 56640273:56640273(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs758705927
CDS Mutation c.1847T>C
AA Mutation p.Leu616Ser(p.L616S)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 36
Mutation Consequence missense_variant
Transcription ID ENST00000312431
Start 56497428:56497428(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs372733281
CDS Mutation c.13403C>T
AA Mutation p.Pro4468Leu(p.P4468L)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 37
Mutation Consequence missense_variant
Transcription ID ENST00000312431
Start 56631933:56631933(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs756379041
CDS Mutation c.3400C>A
AA Mutation p.Leu1134Met(p.L1134M)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 38
Mutation Consequence missense_variant
Transcription ID ENST00000312431
Start 56482747:56482747(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs747281179
CDS Mutation c.14567G>A
AA Mutation p.Arg4856His(p.R4856H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 39
Mutation Consequence missense_variant
Transcription ID ENST00000312431
Start 56497413:56497413(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs776871988
CDS Mutation c.13418C>T
AA Mutation p.Pro4473Leu(p.P4473L)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 40
Mutation Consequence missense_variant
Transcription ID ENST00000312431
Start 56527698:56527698(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.10946C>T
AA Mutation p.Ala3649Val(p.A3649V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 41
Mutation Consequence missense_variant
Transcription ID ENST00000312431
Start 56600145:56600145(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs755261768
CDS Mutation c.4847G>A
AA Mutation p.Arg1616His(p.R1616H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 42
Mutation Consequence missense_variant
Transcription ID ENST00000312431
Start 56634522:56634522(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2921T>C
AA Mutation p.Val974Ala(p.V974A)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 43
Mutation Consequence synonymous_variant
Transcription ID ENST00000312431
Start 56851587:56851587(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.21C>G
Mutation Classification Silent
Feature Type Transcript
ID 44
Mutation Consequence synonymous_variant
Transcription ID ENST00000312431
Start 56501152:56501152(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs767030375
CDS Mutation c.13053G>A
Mutation Classification Silent
Feature Type Transcript
ID 45
Mutation Consequence synonymous_variant
Transcription ID ENST00000312431
Start 56634479:56634479(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs201509973
CDS Mutation c.2964G>A
Mutation Classification Silent
Feature Type Transcript
ID 46
Mutation Consequence synonymous_variant
Transcription ID ENST00000312431
Start 56529481:56529481(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.10791T>A
Mutation Classification Silent
Feature Type Transcript
ID 47
Mutation Consequence synonymous_variant
Transcription ID ENST00000312431
Start 56489535:56489535(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.14061C>T
Mutation Classification Silent
Feature Type Transcript
ID 48
Mutation Consequence synonymous_variant
Transcription ID ENST00000312431
Start 56572915:56572915(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.6615T>C
Mutation Classification Silent
Feature Type Transcript
ID 49
Mutation Consequence synonymous_variant
Transcription ID ENST00000312431
Start 56463700:56463700(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.15981T>C
Mutation Classification Silent
Feature Type Transcript
ID 50
Mutation Consequence synonymous_variant
Transcription ID ENST00000312431
Start 56463646:56463646(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.16035T>C
Mutation Classification Silent
Feature Type Transcript
ID 51
Mutation Consequence synonymous_variant
Transcription ID ENST00000312431
Start 56497454:56497454(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs552952660
CDS Mutation c.13377G>A
Mutation Classification Silent
Feature Type Transcript
ID 52
Mutation Consequence synonymous_variant
Transcription ID ENST00000312431
Start 56536914:56536914(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.9864C>G
Mutation Classification Silent
Feature Type Transcript
ID 53
Mutation Consequence synonymous_variant
Transcription ID ENST00000312431
Start 56640587:56640587(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs148980773
CDS Mutation c.1533C>T
Mutation Classification Silent
Feature Type Transcript
ID 54
Mutation Consequence synonymous_variant
Transcription ID ENST00000312431
Start 56639483:56639483(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2313C>T
Mutation Classification Silent
Feature Type Transcript
ID 55
Mutation Consequence synonymous_variant
Transcription ID ENST00000312431
Start 56511320:56511320(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.11886C>T
Mutation Classification Silent
Feature Type Transcript
ID 56
Mutation Consequence synonymous_variant
Transcription ID ENST00000312431
Start 56492350:56492350(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.13863G>A
Mutation Classification Silent
Feature Type Transcript
ID 57
Mutation Consequence synonymous_variant
Transcription ID ENST00000312431
Start 56459056:56459056(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs199881276
CDS Mutation c.16563G>A
Mutation Classification Silent
Feature Type Transcript
ID 58
Mutation Consequence synonymous_variant
Transcription ID ENST00000312431
Start 56597881:56597881(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs763190713
CDS Mutation c.5283C>T
Mutation Classification Silent
Feature Type Transcript
ID 59
Mutation Consequence frameshift_variant
Transcription ID ENST00000312431
Start 56517567:56517567(version: GRCh38)
Mutation Type DEL
dbSNP_RS rs756726565
CDS Mutation c.11412delA
AA Mutation p.Lys3804AsnfsTer2(p.K3804Nfs*2)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 60
Mutation Consequence frameshift_variant
Transcription ID ENST00000312431
Start 56569919:56569919(version: GRCh38)
Mutation Type DEL
dbSNP_RS null
CDS Mutation c.7044delA
AA Mutation p.Val2349PhefsTer13(p.V2349Ffs*13)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 61
Mutation Consequence frameshift_variant
Transcription ID ENST00000312431
Start 56634897:56634897(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.2730delA
AA Mutation p.Ala911GlnfsTer4(p.A911Qfs*4)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 62
Mutation Consequence frameshift_variant
Transcription ID ENST00000312431
Start 56611526:56611526(version: GRCh38)
Mutation Type DEL
dbSNP_RS rs35805169
CDS Mutation c.4616delT
AA Mutation p.Leu1539TrpfsTer8(p.L1539Wfs*8)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 63
Mutation Consequence frameshift_variant
Transcription ID ENST00000312431
Start 56526557:56526557(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.11162delA
AA Mutation p.Lys3721ArgfsTer16(p.K3721Rfs*16)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 64
Mutation Consequence frameshift_variant
Transcription ID ENST00000312431
Start 56509667:56509667(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.12216delG
AA Mutation p.Thr4073LeufsTer38(p.T4073Lfs*38)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 65
Mutation Consequence frameshift_variant
Transcription ID ENST00000312431
Start 56557468:56557468(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.7720delC
AA Mutation p.Leu2574TrpfsTer8(p.L2574Wfs*8)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 66
Mutation Consequence stop_gained
Transcription ID ENST00000312431
Start 56526429:56526429(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.11290C>T
AA Mutation p.Arg3764Ter(p.R3764*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript
ID 67
Mutation Consequence stop_gained
Transcription ID ENST00000312431
Start 56640207:56640207(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1913T>G
AA Mutation p.Leu638Ter(p.L638*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript
ID 68
Mutation Consequence stop_gained
Transcription ID ENST00000312431
Start 56494117:56494117(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.13516C>T
AA Mutation p.Gln4506Ter(p.Q4506*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript
ID 69
Mutation Consequence stop_gained
Transcription ID ENST00000312431
Start 56460227:56460227(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.16255C>T
AA Mutation p.Arg5419Ter(p.R5419*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript
ID 70
Mutation Consequence stop_gained
Transcription ID ENST00000312431
Start 56634484:56634484(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2959G>T
AA Mutation p.Glu987Ter(p.E987*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript
ID 71
Mutation Consequence stop_gained
Transcription ID ENST00000312431
Start 56593942:56593942(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.5676G>A
AA Mutation p.Trp1892Ter(p.W1892*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript
ID 72
Mutation Consequence stop_gained
Transcription ID ENST00000312431
Start 56552306:56552306(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.9715G>T
AA Mutation p.Glu3239Ter(p.E3239*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript
ID 73
Mutation Consequence frameshift_variant
Transcription ID ENST00000312431
Start 56851456:56851457(version: GRCh38)
Mutation Type INS
dbSNP_RS novel
CDS Mutation c.151dupA
AA Mutation p.Arg51LysfsTer22(p.R51Kfs*22)
Mutation Classification Frame_Shift_Ins
Feature Type Transcript
ID 74
Mutation Consequence splice_acceptor_variant
Transcription ID ENST00000312431
Start 56535293:56535293(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.10000-1G>T
Mutation Classification Splice_Site
Feature Type Transcript