Primary Site >> Stomach Cancer

Gene >> SETBP1

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000282030
Start 44701674:44701674(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.328A>G
AA Mutation p.Thr110Ala(p.T110A)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000282030
Start 44951450:44951450(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2110G>A
AA Mutation p.Ala704Thr(p.A704T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000282030
Start 44952170:44952170(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2830A>C
AA Mutation p.Ser944Arg(p.S944R)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000282030
Start 44701545:44701545(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.199C>T
AA Mutation p.Arg67Trp(p.R67W)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000282030
Start 44951220:44951220(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs138819848
CDS Mutation c.1880G>A
AA Mutation p.Arg627His(p.R627H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000282030
Start 44950080:44950080(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.740G>C
AA Mutation p.Ser247Thr(p.S247T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 7
Mutation Consequence missense_variant
Transcription ID ENST00000282030
Start 44952636:44952636(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3296C>A
AA Mutation p.Ser1099Tyr(p.S1099Y)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 8
Mutation Consequence missense_variant
Transcription ID ENST00000282030
Start 44950797:44950797(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1457C>T
AA Mutation p.Ala486Val(p.A486V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 9
Mutation Consequence missense_variant
Transcription ID ENST00000282030
Start 44951649:44951649(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2309C>T
AA Mutation p.Ala770Val(p.A770V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 10
Mutation Consequence missense_variant
Transcription ID ENST00000282030
Start 44952363:44952363(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs760902522
CDS Mutation c.3023G>A
AA Mutation p.Arg1008His(p.R1008H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 11
Mutation Consequence missense_variant
Transcription ID ENST00000282030
Start 44701746:44701746(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.400A>G
AA Mutation p.Lys134Glu(p.K134E)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 12
Mutation Consequence missense_variant
Transcription ID ENST00000282030
Start 44952092:44952092(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs757255318
CDS Mutation c.2752C>T
AA Mutation p.Arg918Trp(p.R918W)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 13
Mutation Consequence missense_variant
Transcription ID ENST00000282030
Start 45063217:45063217(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.4310A>G
AA Mutation p.Lys1437Arg(p.K1437R)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 14
Mutation Consequence missense_variant
Transcription ID ENST00000282030
Start 44953263:44953263(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3923C>T
AA Mutation p.Thr1308Met(p.T1308M)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 15
Mutation Consequence missense_variant
Transcription ID ENST00000282030
Start 44951520:44951520(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2180G>A
AA Mutation p.Arg727Gln(p.R727Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 16
Mutation Consequence missense_variant
Transcription ID ENST00000282030
Start 44951895:44951895(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs773328311
CDS Mutation c.2555C>T
AA Mutation p.Thr852Met(p.T852M)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 17
Mutation Consequence missense_variant
Transcription ID ENST00000282030
Start 44952396:44952396(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs140544874
CDS Mutation c.3056G>A
AA Mutation p.Arg1019His(p.R1019H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 18
Mutation Consequence missense_variant
Transcription ID ENST00000282030
Start 44701554:44701554(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.208G>T
AA Mutation p.Asp70Tyr(p.D70Y)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 19
Mutation Consequence missense_variant
Transcription ID ENST00000282030
Start 44952520:44952520(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3180G>A
AA Mutation p.Met1060Ile(p.M1060I)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 20
Mutation Consequence missense_variant
Transcription ID ENST00000282030
Start 44953052:44953052(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs144087649
CDS Mutation c.3712G>A
AA Mutation p.Asp1238Asn(p.D1238N)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 21
Mutation Consequence missense_variant
Transcription ID ENST00000282030
Start 44701560:44701560(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.214A>C
AA Mutation p.Asn72His(p.N72H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 22
Mutation Consequence missense_variant
Transcription ID ENST00000282030
Start 44951433:44951433(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2093C>A
AA Mutation p.Thr698Asn(p.T698N)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 23
Mutation Consequence missense_variant
Transcription ID ENST00000282030
Start 44951832:44951832(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2492C>A
AA Mutation p.Pro831Gln(p.P831Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 24
Mutation Consequence missense_variant
Transcription ID ENST00000282030
Start 44952321:44952321(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2981A>G
AA Mutation p.Tyr994Cys(p.Y994C)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 25
Mutation Consequence missense_variant
Transcription ID ENST00000282030
Start 44952326:44952326(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2986G>A
AA Mutation p.Val996Met(p.V996M)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 26
Mutation Consequence missense_variant
Transcription ID ENST00000282030
Start 45063670:45063670(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.4763G>A
AA Mutation p.Arg1588Gln(p.R1588Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 27
Mutation Consequence missense_variant
Transcription ID ENST00000282030
Start 44951343:44951343(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2003A>C
AA Mutation p.Lys668Thr(p.K668T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 28
Mutation Consequence missense_variant
Transcription ID ENST00000282030
Start 44949994:44949994(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.654C>A
AA Mutation p.Asn218Lys(p.N218K)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 29
Mutation Consequence missense_variant
Transcription ID ENST00000282030
Start 44952905:44952905(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3565C>T
AA Mutation p.Arg1189Trp(p.R1189W)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 30
Mutation Consequence missense_variant
Transcription ID ENST00000282030
Start 44950126:44950126(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.786G>T
AA Mutation p.Lys262Asn(p.K262N)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 31
Mutation Consequence missense_variant
Transcription ID ENST00000282030
Start 44951420:44951420(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2080G>T
AA Mutation p.Ala694Ser(p.A694S)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 32
Mutation Consequence synonymous_variant
Transcription ID ENST00000282030
Start 44951575:44951575(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2235C>T
Mutation Classification Silent
Feature Type Transcript
ID 33
Mutation Consequence synonymous_variant
Transcription ID ENST00000282030
Start 44951584:44951584(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2244C>T
Mutation Classification Silent
Feature Type Transcript
ID 34
Mutation Consequence synonymous_variant
Transcription ID ENST00000282030
Start 44951722:44951722(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2382C>T
Mutation Classification Silent
Feature Type Transcript
ID 35
Mutation Consequence synonymous_variant
Transcription ID ENST00000282030
Start 44950108:44950108(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.768C>A
Mutation Classification Silent
Feature Type Transcript
ID 36
Mutation Consequence synonymous_variant
Transcription ID ENST00000282030
Start 44952061:44952061(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs148632511
CDS Mutation c.2721C>T
Mutation Classification Silent
Feature Type Transcript
ID 37
Mutation Consequence synonymous_variant
Transcription ID ENST00000282030
Start 44950510:44950510(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs8091231
CDS Mutation c.1170C>T
Mutation Classification Silent
Feature Type Transcript
ID 38
Mutation Consequence synonymous_variant
Transcription ID ENST00000282030
Start 44950327:44950327(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs371212525
CDS Mutation c.987T>C
Mutation Classification Silent
Feature Type Transcript
ID 39
Mutation Consequence synonymous_variant
Transcription ID ENST00000282030
Start 44951953:44951953(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2613T>C
Mutation Classification Silent
Feature Type Transcript
ID 40
Mutation Consequence synonymous_variant
Transcription ID ENST00000282030
Start 44953132:44953132(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3792T>G
Mutation Classification Silent
Feature Type Transcript
ID 41
Mutation Consequence synonymous_variant
Transcription ID ENST00000282030
Start 45038546:45038546(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.4062A>C
Mutation Classification Silent
Feature Type Transcript
ID 42
Mutation Consequence synonymous_variant
Transcription ID ENST00000282030
Start 44951941:44951941(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs376371660
CDS Mutation c.2601C>T
Mutation Classification Silent
Feature Type Transcript
ID 43
Mutation Consequence synonymous_variant
Transcription ID ENST00000282030
Start 45063134:45063134(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs200760583
CDS Mutation c.4227C>T
Mutation Classification Silent
Feature Type Transcript
ID 44
Mutation Consequence synonymous_variant
Transcription ID ENST00000282030
Start 44952934:44952934(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs200032059
CDS Mutation c.3594G>A
Mutation Classification Silent
Feature Type Transcript
ID 45
Mutation Consequence synonymous_variant
Transcription ID ENST00000282030
Start 44951551:44951551(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2211C>A
Mutation Classification Silent
Feature Type Transcript
ID 46
Mutation Consequence synonymous_variant
Transcription ID ENST00000282030
Start 44951167:44951167(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs140403091
CDS Mutation c.1827C>T
Mutation Classification Silent
Feature Type Transcript
ID 47
Mutation Consequence frameshift_variant
Transcription ID ENST00000282030
Start 44950595:44950595(version: GRCh38)
Mutation Type DEL
dbSNP_RS null
CDS Mutation c.1261delA
AA Mutation p.Arg421AspfsTer23(p.R421Dfs*23)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 48
Mutation Consequence frameshift_variant
Transcription ID ENST00000282030
Start 45063645:45063645(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.4740delA
AA Mutation p.Ala1581ProfsTer30(p.A1581Pfs*30)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 49
Mutation Consequence frameshift_variant
Transcription ID ENST00000282030
Start 44701755:44701755(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.412delG
AA Mutation p.Asp138ThrfsTer69(p.D138Tfs*69)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 50
Mutation Consequence frameshift_variant
Transcription ID ENST00000282030
Start 44701781:44701781(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.440delA
AA Mutation p.Asn147IlefsTer60(p.N147Ifs*60)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 51
Mutation Consequence stop_gained
Transcription ID ENST00000282030
Start 45063669:45063669(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.4762C>T
AA Mutation p.Arg1588Ter(p.R1588*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript
ID 52
Mutation Consequence stop_gained
Transcription ID ENST00000282030
Start 44952695:44952695(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3355G>T
AA Mutation p.Gly1119Ter(p.G1119*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript
ID 53
Mutation Consequence frameshift_variant
Transcription ID ENST00000282030
Start 44869241:44869242(version: GRCh38)
Mutation Type INS
dbSNP_RS novel
CDS Mutation c.500_503dupGTGA
AA Mutation p.Asp168GlufsTer2(p.D168Efs*2)
Mutation Classification Frame_Shift_Ins
Feature Type Transcript
ID 54
Mutation Consequence frameshift_variant
Transcription ID ENST00000282030
Start 44953234:44953235(version: GRCh38)
Mutation Type INS
dbSNP_RS novel
CDS Mutation c.3898dupA
AA Mutation p.Arg1300LysfsTer5(p.R1300Kfs*5)
Mutation Classification Frame_Shift_Ins
Feature Type Transcript
ID 55
Mutation Consequence frameshift_variant
Transcription ID ENST00000282030
Start 44950594:44950595(version: GRCh38)
Mutation Type INS
dbSNP_RS null
CDS Mutation c.1261dupA
AA Mutation p.Arg421LysfsTer5(p.R421Kfs*5)
Mutation Classification Frame_Shift_Ins
Feature Type Transcript
ID 56
Mutation Consequence frameshift_variant
Transcription ID ENST00000282030
Start 44701780:44701781(version: GRCh38)
Mutation Type INS
dbSNP_RS novel
CDS Mutation c.440dupA
AA Mutation p.Asn147LysfsTer2(p.N147Kfs*2)
Mutation Classification Frame_Shift_Ins
Feature Type Transcript