Primary Site >> Esophagus Cancer

Gene >> TLR4

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000355622
Start 117714482:117714482(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2354T>G
AA Mutation p.Leu785Arg(p.L785R)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000355622
Start 117712933:117712933(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.805T>G
AA Mutation p.Leu269Val(p.L269V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000355622
Start 117713620:117713620(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1492T>G
AA Mutation p.Leu498Val(p.L498V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000355622
Start 117714184:117714184(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2056G>T
AA Mutation p.Asp686Tyr(p.D686Y)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000355622
Start 117714392:117714392(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2264A>C
AA Mutation p.Gln755Pro(p.Q755P)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000355622
Start 117713529:117713529(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1401C>A
AA Mutation p.Phe467Leu(p.F467L)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 7
Mutation Consequence synonymous_variant
Transcription ID ENST00000355622
Start 117713304:117713304(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1176T>C
Mutation Classification Silent
Feature Type Transcript