Primary Site >> Esophagus Cancer

Gene >> HLA-B

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000412585
Start 31354502:31354502(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1070A>C
AA Mutation p.Asp357Ala(p.D357A)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000412585
Start 31355385:31355385(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.827G>T
AA Mutation p.Gly276Val(p.G276V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence synonymous_variant
Transcription ID ENST00000412585
Start 31356836:31356836(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.195G>C
Mutation Classification Silent
Feature Type Transcript
ID 4
Mutation Consequence splice_donor_variant
Transcription ID ENST00000412585
Start 31356686:31356686(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.343+2T>C
Mutation Classification Splice_Site
Feature Type Transcript
ID 5
Mutation Consequence splice_donor_variant
Transcription ID ENST00000412585
Start 31356687:31356687(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.343+1G>T
Mutation Classification Splice_Site
Feature Type Transcript