Primary Site >> Stomach Cancer

Gene >> TFCP2

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000257915
Start 51099726:51099726(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1205G>T
AA Mutation p.Arg402Met(p.R402M)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence synonymous_variant
Transcription ID ENST00000257915
Start 51098887:51098887(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1308A>G
Mutation Classification Silent
Feature Type Transcript
ID 3
Mutation Consequence frameshift_variant
Transcription ID ENST00000257915
Start 51107304:51107304(version: GRCh38)
Mutation Type DEL
dbSNP_RS null
CDS Mutation c.760delA
AA Mutation p.Met254TrpfsTer105(p.M254Wfs*105)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 4
Mutation Consequence stop_gained
Transcription ID ENST00000257915
Start 51117730:51117730(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.292C>T
AA Mutation p.Arg98Ter(p.R98*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence splice_donor_variant
Transcription ID ENST00000257915
Start 51109119:51109119(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.717+2T>C
Mutation Classification Splice_Site
Feature Type Transcript