Primary Site >> Stomach Cancer

Gene >> IFIT1

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000371804
Start 89403197:89403197(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.922G>T
AA Mutation p.Gly308Trp(p.G308W)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000371804
Start 89402810:89402810(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.535G>A
AA Mutation p.Ala179Thr(p.A179T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000371804
Start 89402753:89402753(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.478G>A
AA Mutation p.Ala160Thr(p.A160T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence synonymous_variant
Transcription ID ENST00000371804
Start 89402362:89402362(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs779730712
CDS Mutation c.87C>T
Mutation Classification Silent
Feature Type Transcript
ID 5
Mutation Consequence frameshift_variant
Transcription ID ENST00000371804
Start 89403276:89403276(version: GRCh38)
Mutation Type DEL
dbSNP_RS null
CDS Mutation c.1007delA
AA Mutation p.Lys336SerfsTer9(p.K336Sfs*9)
Mutation Classification Frame_Shift_Del
Feature Type Transcript