Primary Site >> Stomach Cancer

Gene >> TARBP2

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000266987
Start 53504758:53504758(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.556C>T
AA Mutation p.Pro186Ser(p.P186S)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000266987
Start 53505661:53505661(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.754C>T
AA Mutation p.Arg252Cys(p.R252C)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence synonymous_variant
Transcription ID ENST00000266987
Start 53506130:53506130(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1083C>T
Mutation Classification Silent
Feature Type Transcript
ID 4
Mutation Consequence synonymous_variant
Transcription ID ENST00000266987
Start 53506040:53506040(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.993C>T
Mutation Classification Silent
Feature Type Transcript
ID 5
Mutation Consequence synonymous_variant
Transcription ID ENST00000266987
Start 53503776:53503776(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.390T>A
Mutation Classification Silent
Feature Type Transcript
ID 6
Mutation Consequence splice_donor_variant
Transcription ID ENST00000266987
Start 53505852:53505852(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.943+2T>C
Mutation Classification Splice_Site
Feature Type Transcript