Primary Site >> Esophagus Cancer

Gene >> PHB

ID 1
Mutation Consequence splice_acceptor_variant
Transcription ID ENST00000300408
Start 49409159:49409159(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.394-1G>T
Mutation Classification Splice_Site
Feature Type Transcript
ID 2
Mutation Consequence splice_acceptor_variant
Transcription ID ENST00000300408
Start 49411840:49411841(version: GRCh38)
Mutation Type INS
dbSNP_RS novel
CDS Mutation c.89-2_89-1insT
Mutation Classification Splice_Site
Feature Type Transcript