Primary Site >> Stomach Cancer

Gene >> TTK

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000369798
Start 80022401:80022401(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1186A>T
AA Mutation p.Ile396Phe(p.I396F)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000369798
Start 80007937:80007937(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.268C>T
AA Mutation p.Arg90Cys(p.R90C)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000369798
Start 80013361:80013361(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.979T>A
AA Mutation p.Leu327Ile(p.L327I)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000369798
Start 80014512:80014512(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs200901836
CDS Mutation c.1034G>A
AA Mutation p.Ser345Asn(p.S345N)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000369798
Start 80040660:80040660(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2447T>G
AA Mutation p.Leu816Arg(p.L816R)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000369798
Start 80007938:80007938(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs376160183
CDS Mutation c.269G>A
AA Mutation p.Arg90His(p.R90H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 7
Mutation Consequence missense_variant
Transcription ID ENST00000369798
Start 80035354:80035354(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1861C>T
AA Mutation p.Pro621Ser(p.P621S)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 8
Mutation Consequence missense_variant
Transcription ID ENST00000369798
Start 80008486:80008486(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.463T>A
AA Mutation p.Ser155Thr(p.S155T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 9
Mutation Consequence synonymous_variant
Transcription ID ENST00000369798
Start 80042154:80042154(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2526T>C
Mutation Classification Silent
Feature Type Transcript
ID 10
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
ID 11
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
ID 12
Mutation Consequence frameshift_variant
Transcription ID ENST00000369798
Start 80042193:80042193(version: GRCh38)
Mutation Type DEL
dbSNP_RS rs768996038
CDS Mutation c.2571delA
AA Mutation p.Lys857AsnfsTer36(p.K857Nfs*36)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 13
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
ID 14
Mutation Consequence frameshift_variant
Transcription ID ENST00000369798
Start 80007860:80007879(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.192_211delCTGGTTGAGTTTGTTGCTCA
AA Mutation p.Asp64GlufsTer11(p.D64Efs*11)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 15
Mutation Consequence stop_gained
Transcription ID ENST00000369798
Start 80013301:80013301(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.919C>T
AA Mutation p.Arg307Ter(p.R307*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript
ID 16
Mutation Consequence splice_acceptor_variant
Transcription ID ENST00000369798
Start 80011885:80011885(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.802-1G>A
Mutation Classification Splice_Site
Feature Type Transcript
ID 17
Mutation Consequence splice_donor_variant
Transcription ID ENST00000369798
Start 80040282:80040282(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2392+2T>C
Mutation Classification Splice_Site
Feature Type Transcript