Primary Site >> Esophagus Cancer

Gene >> TRIM33

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000358465
Start 114464379:114464379(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.536T>G
AA Mutation p.Ile179Arg(p.I179R)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence synonymous_variant
Transcription ID ENST00000358465
Start 114397961:114397961(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.3150C>T
Mutation Classification Silent
Feature Type Transcript