Primary Site >> Stomach Cancer

Gene >> TFPT

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000391759
Start 54108355:54108355(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs148303725
CDS Mutation c.394C>T
AA Mutation p.Arg132Trp(p.R132W)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000391759
Start 54108045:54108045(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.623C>T
AA Mutation p.Pro208Leu(p.P208L)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000391759
Start 54114693:54114693(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.31G>A
AA Mutation p.Ala11Thr(p.A11T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence synonymous_variant
Transcription ID ENST00000391759
Start 54108236:54108236(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.432C>T
Mutation Classification Silent
Feature Type Transcript
ID 5
Mutation Consequence synonymous_variant
Transcription ID ENST00000391759
Start 54114685:54114685(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.39G>T
Mutation Classification Silent
Feature Type Transcript