Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> TNIK

Mutation ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000436636
Start 171084267:171084267(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3057G>T
AA Mutation p.Lys1019Asn(p.K1019N)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000436636
Start 171082343:171082343(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3221G>C
AA Mutation p.Ser1074Thr(p.S1074T)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000436636
Start 171175286:171175286(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.739C>T
AA Mutation p.Arg247Trp(p.R247W)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000436636
Start 171128838:171128838(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1649C>T
AA Mutation p.Ala550Val(p.A550V)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000436636
Start 171190781:171190781(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.424A>G
AA Mutation p.Ser142Gly(p.S142G)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000436636
Start 171194571:171194571(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.371C>A
AA Mutation p.Thr124Lys(p.T124K)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 7
Mutation Consequence missense_variant
Transcription ID ENST00000436636
Start 171123611:171123611(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2105A>C
AA Mutation p.Gln702Pro(p.Q702P)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 8
Mutation Consequence missense_variant
Transcription ID ENST00000436636
Start 171066719:171066719(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.3716C>T
AA Mutation p.Thr1239Ile(p.T1239I)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 9
Mutation Consequence missense_variant
Transcription ID ENST00000436636
Start 171140418:171140418(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1313G>T
AA Mutation p.Arg438Met(p.R438M)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 10
Mutation Consequence missense_variant;splice_region_variant
Transcription ID ENST00000436636
Start 171194527:171194527(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs772057234
CDS Mutation c.415C>T
AA Mutation p.Arg139Trp(p.R139W)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 11
Mutation Consequence missense_variant
Transcription ID ENST00000436636
Start 171167173:171167173(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.871G>A
AA Mutation p.Asp291Asn(p.D291N)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 12
Mutation Consequence missense_variant
Transcription ID ENST00000436636
Start 171066726:171066726(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.3709A>G
AA Mutation p.Asn1237Asp(p.N1237D)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 13
Mutation Consequence missense_variant
Transcription ID ENST00000436636
Start 171139540:171139540(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1349A>C
AA Mutation p.Gln450Pro(p.Q450P)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 14
Mutation Consequence missense_variant
Transcription ID ENST00000436636
Start 171108129:171108129(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2318C>T
AA Mutation p.Pro773Leu(p.P773L)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 15
Mutation Consequence missense_variant
Transcription ID ENST00000436636
Start 171084307:171084307(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3017T>C
AA Mutation p.Leu1006Pro(p.L1006P)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 16
Mutation Consequence missense_variant
Transcription ID ENST00000436636
Start 171190739:171190739(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.466G>T
AA Mutation p.Gly156Trp(p.G156W)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 17
Mutation Consequence missense_variant
Transcription ID ENST00000436636
Start 171190738:171190738(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.467G>A
AA Mutation p.Gly156Glu(p.G156E)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 18
Mutation Consequence missense_variant
Transcription ID ENST00000436636
Start 171084262:171084262(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3062C>T
AA Mutation p.Ser1021Leu(p.S1021L)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 19
Mutation Consequence missense_variant
Transcription ID ENST00000436636
Start 171066679:171066679(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.3756G>C
AA Mutation p.Met1252Ile(p.M1252I)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 20
Mutation Consequence synonymous_variant
Transcription ID ENST00000436636
Start 171460055:171460055(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.9C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 21
Mutation Consequence synonymous_variant
Transcription ID ENST00000436636
Start 171101496:171101496(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs769724807
CDS Mutation c.2544C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 22
Mutation Consequence synonymous_variant
Transcription ID ENST00000436636
Start 171126107:171126107(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs779458498
CDS Mutation c.1818C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 23
Mutation Consequence synonymous_variant
Transcription ID ENST00000436636
Start 171108107:171108107(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2340A>G
Mutation Classification Silent
Feature Type Transcript
Mutation ID 24
Mutation Consequence synonymous_variant
Transcription ID ENST00000436636
Start 171110787:171110787(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2211C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 25
Mutation Consequence synonymous_variant
Transcription ID ENST00000436636
Start 171101523:171101523(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs542453210
CDS Mutation c.2517C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 26
Mutation Consequence frameshift_variant
Transcription ID ENST00000436636
Start 171167261:171167261(version: GRCh38)
Mutation Type DEL
dbSNP_RS null
CDS Mutation c.783delA
AA Mutation p.Lys261AsnfsTer11(p.K261Nfs*11)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
Mutation ID 27
Mutation Consequence frameshift_variant
Transcription ID ENST00000436636
Start 171066648:171066648(version: GRCh38)
Mutation Type DEL
dbSNP_RS null
CDS Mutation c.3787delG
AA Mutation p.Val1263CysfsTer3(p.V1263Cfs*3)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
Mutation ID 28
Mutation Consequence frameshift_variant
Transcription ID ENST00000436636
Start 171063956:171063956(version: GRCh38)
Mutation Type DEL
dbSNP_RS null
CDS Mutation c.4008delT
AA Mutation p.Phe1336LeufsTer15(p.F1336Lfs*15)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
Mutation ID 29
Mutation Consequence frameshift_variant
Transcription ID ENST00000436636
Start 171066678:171066678(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.3757delG
AA Mutation p.Glu1253LysfsTer13(p.E1253Kfs*13)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
Mutation ID 30
Mutation Consequence stop_gained
Transcription ID ENST00000436636
Start 171063946:171063946(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.4018C>T
AA Mutation p.Arg1340Ter(p.R1340*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript
Mutation ID 31
Mutation Consequence stop_gained
Transcription ID ENST00000436636
Start 171167101:171167101(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.943G>T
AA Mutation p.Glu315Ter(p.E315*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript
Mutation ID 32
Mutation Consequence stop_gained
Transcription ID ENST00000436636
Start 171110717:171110717(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2281C>T
AA Mutation p.Arg761Ter(p.R761*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript
Mutation ID 33
Mutation Consequence frameshift_variant
Transcription ID ENST00000436636
Start 171211146:171211147(version: GRCh38)
Mutation Type INS
dbSNP_RS null
CDS Mutation c.275dupA
AA Mutation p.Asn93GlufsTer7(p.N93Efs*7)
Mutation Classification Frame_Shift_Ins
Feature Type Transcript
Mutation ID 34
Mutation Consequence frameshift_variant
Transcription ID ENST00000436636
Start 171128809:171128810(version: GRCh38)
Mutation Type INS
dbSNP_RS novel
CDS Mutation c.1677dupA
AA Mutation p.Ser560IlefsTer2(p.S560Ifs*2)
Mutation Classification Frame_Shift_Ins
Feature Type Transcript

Rectum Cancer: Gene >> TNIK

Mutation ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000436636
Start 171167220:171167220(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.824G>T
AA Mutation p.Ser275Ile(p.S275I)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000436636
Start 171128782:171128782(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1705G>A
AA Mutation p.Glu569Lys(p.E569K)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000436636
Start 171194604:171194604(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.338T>C
AA Mutation p.Val113Ala(p.V113A)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000436636
Start 171063951:171063951(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.4013C>T
AA Mutation p.Ser1338Phe(p.S1338F)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 5
Mutation Consequence missense_variant;splice_region_variant
Transcription ID ENST00000436636
Start 171068996:171068996(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3551C>A
AA Mutation p.Ser1184Tyr(p.S1184Y)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000436636
Start 171063958:171063958(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.4006T>G
AA Mutation p.Phe1336Val(p.F1336V)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 7
Mutation Consequence synonymous_variant
Transcription ID ENST00000436636
Start 171167111:171167111(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.933G>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 8
Mutation Consequence frameshift_variant
Transcription ID ENST00000436636
Start 171063956:171063956(version: GRCh38)
Mutation Type DEL
dbSNP_RS null
CDS Mutation c.4008delT
AA Mutation p.Phe1336LeufsTer15(p.F1336Lfs*15)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
Mutation ID 9
Mutation Consequence stop_gained
Transcription ID ENST00000436636
Start 171110717:171110717(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2281C>T
AA Mutation p.Arg761Ter(p.R761*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript
Mutation ID 10
Mutation Consequence stop_gained
Transcription ID ENST00000436636
Start 171167101:171167101(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.943G>T
AA Mutation p.Glu315Ter(p.E315*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript