Primary Site >> Esophagus Cancer

Gene >> FAIM

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000393034
Start 138622266:138622266(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.190A>G
AA Mutation p.Thr64Ala(p.T64A)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence synonymous_variant
Transcription ID ENST00000393034
Start 138621437:138621437(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.9T>C
Mutation Classification Silent
Feature Type Transcript