Primary Site >> Esophagus Cancer

Gene >> BRD4

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000263377
Start 15256163:15256163(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1652A>G
AA Mutation p.His551Arg(p.H551R)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000263377
Start 15256199:15256199(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1616A>G
AA Mutation p.Lys539Arg(p.K539R)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000263377
Start 15255507:15255507(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1837G>A
AA Mutation p.Glu613Lys(p.E613K)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000263377
Start 15265503:15265503(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.700G>A
AA Mutation p.Val234Ile(p.V234I)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000263377
Start 15244366:15244366(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs760576705
CDS Mutation c.2446G>A
AA Mutation p.Val816Ile(p.V816I)
Mutation Classification Missense_Mutation
Feature Type Transcript