Primary Site >> Stomach Cancer

Gene >> IRF9

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000396864
Start 24162973:24162973(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.188C>A
AA Mutation p.Ala63Glu(p.A63E)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000396864
Start 24162194:24162194(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.50T>C
AA Mutation p.Val17Ala(p.V17A)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000396864
Start 24164649:24164649(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.685C>T
AA Mutation p.Arg229Cys(p.R229C)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000396864
Start 24164857:24164857(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.893T>C
AA Mutation p.Ile298Thr(p.I298T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence synonymous_variant
Transcription ID ENST00000396864
Start 24164687:24164687(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.723C>T
Mutation Classification Silent
Feature Type Transcript
ID 6
Mutation Consequence synonymous_variant
Transcription ID ENST00000396864
Start 24164625:24164625(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.661C>T
Mutation Classification Silent
Feature Type Transcript
ID 7
Mutation Consequence frameshift_variant
Transcription ID ENST00000396864
Start 24165875:24165875(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.1025delC
AA Mutation p.Pro342HisfsTer6(p.P342Hfs*6)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 8
Mutation Consequence inframe_deletion
Transcription ID ENST00000396864
Start 24164633:24164635(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.670_672delTTC
AA Mutation p.Phe224del(p.F224del)
Mutation Classification In_Frame_Del
Feature Type Transcript