Primary Site >> Esophagus Cancer

Gene >> PBX1

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000420696
Start 164821561:164821561(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1135A>G
AA Mutation p.Ser379Gly(p.S379G)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000420696
Start 164559886:164559886(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.64C>A
AA Mutation p.Leu22Met(p.L22M)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000420696
Start 164559908:164559908(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.86G>T
AA Mutation p.Gly29Val(p.G29V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence synonymous_variant
Transcription ID ENST00000420696
Start 164820106:164820106(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1032A>T
Mutation Classification Silent
Feature Type Transcript