Primary Site >> Stomach Cancer

Gene >> TFR2

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000223051
Start 100629280:100629280(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs749498767
CDS Mutation c.1363C>T
AA Mutation p.Arg455Trp(p.R455W)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence synonymous_variant
Transcription ID ENST00000223051
Start 100620896:100620896(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs374766778
CDS Mutation c.2367G>A
Mutation Classification Silent
Feature Type Transcript
ID 3
Mutation Consequence synonymous_variant
Transcription ID ENST00000223051
Start 100631007:100631007(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1152C>T
Mutation Classification Silent
Feature Type Transcript
ID 4
Mutation Consequence frameshift_variant;splice_region_variant
Transcription ID ENST00000223051
Start 100633114:100633121(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.729_736delAGAGCTGG
AA Mutation p.Glu244ValfsTer196(p.E244Vfs*196)
Mutation Classification Frame_Shift_Del
Feature Type Transcript