Primary Site >> Esophagus Cancer

Gene >> SELL

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000236147
Start 169708578:169708578(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.350A>C
AA Mutation p.Asn117Thr(p.N117T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence synonymous_variant
Transcription ID ENST00000236147
Start 169701615:169701615(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1065T>C
Mutation Classification Silent
Feature Type Transcript