Primary Site >> Esophagus Cancer

Gene >> APP

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000346798
Start 25975107:25975107(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1421A>G
AA Mutation p.Glu474Gly(p.E474G)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000346798
Start 26089980:26089980(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.318G>T
AA Mutation p.Lys106Asn(p.K106N)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence synonymous_variant
Transcription ID ENST00000346798
Start 25891794:25891794(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs749919142
CDS Mutation c.2139G>A
Mutation Classification Silent
Feature Type Transcript
ID 4
Mutation Consequence synonymous_variant
Transcription ID ENST00000346798
Start 26051140:26051140(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs199905579
CDS Mutation c.522C>T
Mutation Classification Silent
Feature Type Transcript