Primary Site >> Esophagus Cancer

Gene >> SEMG2

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000372769
Start 45222767:45222767(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1135G>A
AA Mutation p.Glu379Lys(p.E379K)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000372769
Start 45222507:45222507(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs145586123
CDS Mutation c.875G>A
AA Mutation p.Arg292His(p.R292H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence synonymous_variant
Transcription ID ENST00000372769
Start 45222001:45222001(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.369T>C
Mutation Classification Silent
Feature Type Transcript
ID 4
Mutation Consequence synonymous_variant
Transcription ID ENST00000372769
Start 45223210:45223210(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1578G>A
Mutation Classification Silent
Feature Type Transcript