Primary Site >> Esophagus Cancer

Gene >> SBSN

ID 1
Mutation Consequence synonymous_variant
Transcription ID ENST00000452271
Start 35527169:35527169(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1113G>A
Mutation Classification Silent
Feature Type Transcript
ID 2
Mutation Consequence frameshift_variant
Transcription ID ENST00000452271
Start 35527021:35527022(version: GRCh38)
Mutation Type INS
dbSNP_RS null
CDS Mutation c.1260dupG
AA Mutation p.Gln421AlafsTer47(p.Q421Afs*47)
Mutation Classification Frame_Shift_Ins
Feature Type Transcript