Primary Site >> Esophagus Cancer

Gene >> GCLC

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000229416
Start 53509190:53509190(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.814A>G
AA Mutation p.Ile272Val(p.I272V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence synonymous_variant
Transcription ID ENST00000229416
Start 53498891:53498891(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1779A>C
Mutation Classification Silent
Feature Type Transcript