Primary Site >> Esophagus Cancer

Gene >> PRDM1

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000369096
Start 106105140:106105140(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.980C>G
AA Mutation p.Ser327Cys(p.S327C)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000369096
Start 106088417:106088417(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.259C>A
AA Mutation p.Leu87Met(p.L87M)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence synonymous_variant
Transcription ID ENST00000369096
Start 106105855:106105855(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1695G>A
Mutation Classification Silent
Feature Type Transcript
ID 4
Mutation Consequence synonymous_variant
Transcription ID ENST00000369096
Start 106105603:106105603(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs777578275
CDS Mutation c.1443G>A
Mutation Classification Silent
Feature Type Transcript