Primary Site >> Stomach Cancer

Gene >> TCF7L1

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000282111
Start 85283553:85283553(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs35802950
CDS Mutation c.500C>T
AA Mutation p.Thr167Met(p.T167M)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000282111
Start 85305370:85305370(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs138614113
CDS Mutation c.956C>T
AA Mutation p.Pro319Leu(p.P319L)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000282111
Start 85309389:85309389(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs756969067
CDS Mutation c.1694C>T
AA Mutation p.Thr565Met(p.T565M)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000282111
Start 85309237:85309237(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs764185209
CDS Mutation c.1542G>T
AA Mutation p.Gln514His(p.Q514H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000282111
Start 85309130:85309130(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1435C>A
AA Mutation p.Pro479Thr(p.P479T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence synonymous_variant
Transcription ID ENST00000282111
Start 85134363:85134363(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.354G>A
Mutation Classification Silent
Feature Type Transcript
ID 7
Mutation Consequence stop_retained_variant
Transcription ID ENST00000282111
Start 85309461:85309461(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1766A>G
Mutation Classification Silent
Feature Type Transcript
ID 8
Mutation Consequence frameshift_variant
Transcription ID ENST00000282111
Start 85305375:85305375(version: GRCh38)
Mutation Type DEL
dbSNP_RS null
CDS Mutation c.966delC
AA Mutation p.Ser323AlafsTer2(p.S323Afs*2)
Mutation Classification Frame_Shift_Del
Feature Type Transcript