Primary Site >> Esophagus Cancer

Gene >> TENM2

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000518659
Start 168247979:168247979(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.7040A>G
AA Mutation p.Tyr2347Cys(p.Y2347C)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000518659
Start 168062237:168062237(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1487G>T
AA Mutation p.Arg496Ile(p.R496I)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000518659
Start 168062106:168062106(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1356A>C
AA Mutation p.Glu452Asp(p.E452D)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000518659
Start 168218894:168218894(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.5003A>T
AA Mutation p.Lys1668Ile(p.K1668I)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence synonymous_variant
Transcription ID ENST00000518659
Start 168090582:168090582(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1524C>T
Mutation Classification Silent
Feature Type Transcript