Primary Site >> Stomach Cancer

Gene >> CFP

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000247153
Start 47627144:47627144(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.763C>A
AA Mutation p.Pro255Thr(p.P255T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence synonymous_variant
Transcription ID ENST00000247153
Start 47626437:47626437(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs371351644
CDS Mutation c.1023G>A
Mutation Classification Silent
Feature Type Transcript
ID 3
Mutation Consequence synonymous_variant
Transcription ID ENST00000247153
Start 47627175:47627175(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.732G>A
Mutation Classification Silent
Feature Type Transcript
ID 4
Mutation Consequence stop_gained
Transcription ID ENST00000247153
Start 47626507:47626507(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.953G>A
AA Mutation p.Trp318Ter(p.W318*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript