Primary Site >> Esophagus Cancer

Gene >> NOS2

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000313735
Start 27760675:27760675(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2958C>G
AA Mutation p.Ile986Met(p.I986M)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence synonymous_variant
Transcription ID ENST00000313735
Start 27789610:27789610(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.189G>A
Mutation Classification Silent
Feature Type Transcript
ID 3
Mutation Consequence synonymous_variant
Transcription ID ENST00000313735
Start 27766518:27766518(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs778148076
CDS Mutation c.2238G>A
Mutation Classification Silent
Feature Type Transcript
ID 4
Mutation Consequence synonymous_variant
Transcription ID ENST00000313735
Start 27764110:27764110(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2463C>A
Mutation Classification Silent
Feature Type Transcript