Primary Site >> Esophagus Cancer

Gene >> CNR1

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000369499
Start 88144796:88144796(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs759310920
CDS Mutation c.479C>T
AA Mutation p.Ala160Val(p.A160V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000369499
Start 88144091:88144091(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1184T>A
AA Mutation p.Ile395Asn(p.I395N)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000369499
Start 88144685:88144685(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.590C>T
AA Mutation p.Thr197Met(p.T197M)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence synonymous_variant
Transcription ID ENST00000369499
Start 88145266:88145266(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs371432780
CDS Mutation c.9G>A
Mutation Classification Silent
Feature Type Transcript
ID 5
Mutation Consequence synonymous_variant
Transcription ID ENST00000369499
Start 88145203:88145203(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.72C>T
Mutation Classification Silent
Feature Type Transcript