Primary Site >> Esophagus Cancer

Gene >> ICAM5

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000221980
Start 10291207:10291207(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.218G>A
AA Mutation p.Arg73Gln(p.R73Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000221980
Start 10290119:10290119(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.76C>T
AA Mutation p.Leu26Phe(p.L26F)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000221980
Start 10292266:10292266(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.905G>A
AA Mutation p.Cys302Tyr(p.C302Y)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence synonymous_variant
Transcription ID ENST00000221980
Start 10293233:10293233(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs773640360
CDS Mutation c.1452G>A
Mutation Classification Silent
Feature Type Transcript
ID 5
Mutation Consequence synonymous_variant
Transcription ID ENST00000221980
Start 10292730:10292730(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1080G>A
Mutation Classification Silent
Feature Type Transcript