Primary Site >> Stomach Cancer

Gene >> LEF1

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000265165
Start 108163581:108163581(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.401C>T
AA Mutation p.Pro134Leu(p.P134L)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000265165
Start 108079516:108079516(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.821A>G
AA Mutation p.His274Arg(p.H274R)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000265165
Start 108167641:108167641(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.127C>T
AA Mutation p.His43Tyr(p.H43Y)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000265165
Start 108089220:108089220(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.452T>C
AA Mutation p.Val151Ala(p.V151A)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000265165
Start 108078372:108078372(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.856C>T
AA Mutation p.His286Tyr(p.H286Y)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000265165
Start 108167712:108167712(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.56C>T
AA Mutation p.Ala19Val(p.A19V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 7
Mutation Consequence synonymous_variant
Transcription ID ENST00000265165
Start 108081654:108081654(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.654A>G
Mutation Classification Silent
Feature Type Transcript