Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> TTK

Mutation ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000369798
Start 80035293:80035293(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1800G>T
AA Mutation p.Met600Ile(p.M600I)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000369798
Start 80027906:80027906(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1416G>T
AA Mutation p.Lys472Asn(p.K472N)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000369798
Start 80005930:80005930(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.87T>G
AA Mutation p.Asn29Lys(p.N29K)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000369798
Start 80035113:80035113(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1743C>A
AA Mutation p.His581Gln(p.H581Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000369798
Start 80035364:80035364(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1871G>A
AA Mutation p.Arg624His(p.R624H)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000369798
Start 80022353:80022353(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1138C>G
AA Mutation p.Pro380Ala(p.P380A)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 7
Mutation Consequence missense_variant
Transcription ID ENST00000369798
Start 80035363:80035363(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs200822002
CDS Mutation c.1870C>T
AA Mutation p.Arg624Cys(p.R624C)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 8
Mutation Consequence missense_variant
Transcription ID ENST00000369798
Start 80040624:80040624(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2411G>C
AA Mutation p.Gly804Ala(p.G804A)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 9
Mutation Consequence missense_variant
Transcription ID ENST00000369798
Start 80039735:80039735(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2170T>G
AA Mutation p.Leu724Val(p.L724V)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 10
Mutation Consequence missense_variant
Transcription ID ENST00000369798
Start 80005953:80005953(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.110G>T
AA Mutation p.Ser37Ile(p.S37I)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 11
Mutation Consequence missense_variant
Transcription ID ENST00000369798
Start 80010886:80010886(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.542A>C
AA Mutation p.Glu181Ala(p.E181A)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 12
Mutation Consequence synonymous_variant
Transcription ID ENST00000369798
Start 80014570:80014570(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1092T>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 13
Mutation Consequence frameshift_variant
Transcription ID ENST00000369798
Start 80010913:80010913(version: GRCh38)
Mutation Type DEL
dbSNP_RS null
CDS Mutation c.575delA
AA Mutation p.Lys192SerfsTer18(p.K192Sfs*18)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
Mutation ID 14
Mutation Consequence frameshift_variant
Transcription ID ENST00000369798
Start 80010822:80010822(version: GRCh38)
Mutation Type DEL
dbSNP_RS rs763863683
CDS Mutation c.484delA
AA Mutation p.Ser162ValfsTer9(p.S162Vfs*9)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
Mutation ID 15
Mutation Consequence frameshift_variant
Transcription ID ENST00000369798
Start 80042180:80042181(version: GRCh38)
Mutation Type DEL
dbSNP_RS null
CDS Mutation c.2559_2560delAA
AA Mutation p.Arg854GlyfsTer10(p.R854Gfs*10)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
Mutation ID 16
Mutation Consequence frameshift_variant
Transcription ID ENST00000369798
Start 80042180:80042180(version: GRCh38)
Mutation Type DEL
dbSNP_RS rs763254614
CDS Mutation c.2560delA
AA Mutation p.Arg854GlyfsTer39(p.R854Gfs*39)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
Mutation ID 17
Mutation Consequence frameshift_variant
Transcription ID ENST00000369798
Start 80005951:80005952(version: GRCh38)
Mutation Type INS
dbSNP_RS novel
CDS Mutation c.108_109insGC
AA Mutation p.Ser37AlafsTer3(p.S37Afs*3)
Mutation Classification Frame_Shift_Ins
Feature Type Transcript
Mutation ID 18
Mutation Consequence frameshift_variant
Transcription ID ENST00000369798
Start 80014568:80014569(version: GRCh38)
Mutation Type INS
dbSNP_RS novel
CDS Mutation c.1090_1091insCCATAAATAGTAG
AA Mutation p.Leu364ProfsTer8(p.L364Pfs*8)
Mutation Classification Frame_Shift_Ins
Feature Type Transcript

Rectum Cancer: Gene >> TTK

Mutation ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000369798
Start 80014512:80014512(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1034G>T
AA Mutation p.Ser345Ile(p.S345I)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000369798
Start 80035081:80035081(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs773610148
CDS Mutation c.1711G>A
AA Mutation p.Glu571Lys(p.E571K)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000369798
Start 80007974:80007974(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.305A>C
AA Mutation p.Lys102Thr(p.K102T)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000369798
Start 80008443:80008443(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.420G>T
AA Mutation p.Lys140Asn(p.K140N)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000369798
Start 80028002:80028002(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1512A>C
AA Mutation p.Gln504His(p.Q504H)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000369798
Start 80039736:80039736(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2171T>C
AA Mutation p.Leu724Ser(p.L724S)
Mutation Classification Missense_Mutation
Feature Type Transcript