Primary Site >> Esophagus Cancer

Gene >> CDH2

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000269141
Start 27952245:27952245(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2629A>C
AA Mutation p.Ser877Arg(p.S877R)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000269141
Start 27992747:27992747(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1252G>T
AA Mutation p.Ala418Ser(p.A418S)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000269141
Start 28147730:28147730(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.115G>A
AA Mutation p.Asp39Asn(p.D39N)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence synonymous_variant
Transcription ID ENST00000269141
Start 27963393:27963393(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2478C>A
Mutation Classification Silent
Feature Type Transcript