Primary Site >> Stomach Cancer

Gene >> NLK

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000407008
Start 28043241:28043241(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.368C>T
AA Mutation p.Ala123Val(p.A123V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000407008
Start 28168470:28168470(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.860G>A
AA Mutation p.Arg287Lys(p.R287K)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000407008
Start 28043222:28043222(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.349G>A
AA Mutation p.Ala117Thr(p.A117T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence synonymous_variant
Transcription ID ENST00000407008
Start 28191092:28191092(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1308A>C
Mutation Classification Silent
Feature Type Transcript
ID 5
Mutation Consequence synonymous_variant
Transcription ID ENST00000407008
Start 28191074:28191074(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs755786504
CDS Mutation c.1290G>A
Mutation Classification Silent
Feature Type Transcript
ID 6
Mutation Consequence frameshift_variant
Transcription ID ENST00000407008
Start 28122714:28122714(version: GRCh38)
Mutation Type DEL
dbSNP_RS null
CDS Mutation c.576delT
AA Mutation p.Phe192LeufsTer30(p.F192Lfs*30)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 7
Mutation Consequence stop_gained
Transcription ID ENST00000407008
Start 28191075:28191075(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1291C>T
AA Mutation p.Arg431Ter(p.R431*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript
ID 8
Mutation Consequence frameshift_variant
Transcription ID ENST00000407008
Start 28122713:28122714(version: GRCh38)
Mutation Type INS
dbSNP_RS novel
CDS Mutation c.576dupT
AA Mutation p.Lys193Ter(p.K193*)
Mutation Classification Frame_Shift_Ins
Feature Type Transcript
ID 9
Mutation Consequence inframe_deletion;splice_region_variant
Transcription ID ENST00000407008
Start 28185179:28185184(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.1151_1156delCATCTC
AA Mutation p.Pro384_Ser385del(p.P384_S385del)
Mutation Classification In_Frame_Del
Feature Type Transcript