Primary Site >> Stomach Cancer

Gene >> IKBKE

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000581977
Start 206476823:206476823(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs377576134
CDS Mutation c.686G>A
AA Mutation p.Arg229Gln(p.R229Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000581977
Start 206493988:206493988(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2114A>G
AA Mutation p.Glu705Gly(p.E705G)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000581977
Start 206491674:206491674(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1760G>T
AA Mutation p.Arg587Ile(p.R587I)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000581977
Start 206474419:206474419(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.176T>C
AA Mutation p.Leu59Pro(p.L59P)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000581977
Start 206491656:206491656(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1742T>A
AA Mutation p.Phe581Tyr(p.F581Y)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000581977
Start 206479034:206479034(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs782242787
CDS Mutation c.1084G>A
AA Mutation p.Glu362Lys(p.E362K)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 7
Mutation Consequence missense_variant
Transcription ID ENST00000581977
Start 206476249:206476249(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.427C>T
AA Mutation p.Arg143Cys(p.R143C)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 8
Mutation Consequence missense_variant
Transcription ID ENST00000581977
Start 206478987:206478987(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1037C>T
AA Mutation p.Ala346Val(p.A346V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 9
Mutation Consequence missense_variant
Transcription ID ENST00000581977
Start 206474961:206474961(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.325G>A
AA Mutation p.Glu109Lys(p.E109K)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 10
Mutation Consequence synonymous_variant
Transcription ID ENST00000581977
Start 206496127:206496127(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2133A>G
Mutation Classification Silent
Feature Type Transcript
ID 11
Mutation Consequence frameshift_variant
Transcription ID ENST00000581977
Start 206478987:206478987(version: GRCh38)
Mutation Type DEL
dbSNP_RS null
CDS Mutation c.1042delC
AA Mutation p.Arg348AspfsTer32(p.R348Dfs*32)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 12
Mutation Consequence frameshift_variant
Transcription ID ENST00000581977
Start 206474385:206474385(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.145delC
AA Mutation p.Arg49AlafsTer5(p.R49Afs*5)
Mutation Classification Frame_Shift_Del
Feature Type Transcript