Primary Site >> Esophagus Cancer

Gene >> SLC2A1

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000426263
Start 42929006:42929006(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1000C>T
AA Mutation p.Arg334Trp(p.R334W)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence synonymous_variant
Transcription ID ENST00000426263
Start 42930737:42930737(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.405G>C
Mutation Classification Silent
Feature Type Transcript