Primary Site >> Esophagus Cancer

Gene >> GRN

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000053867
Start 44350524:44350524(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs63750479
CDS Mutation c.545C>T
AA Mutation p.Thr182Met(p.T182M)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000053867
Start 44350727:44350727(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs63750787
CDS Mutation c.635G>A
AA Mutation p.Arg212Gln(p.R212Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000053867
Start 44351429:44351429(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.902C>T
AA Mutation p.Ser301Leu(p.S301L)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence synonymous_variant
Transcription ID ENST00000053867
Start 44350504:44350504(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.525C>T
Mutation Classification Silent
Feature Type Transcript
ID 5
Mutation Consequence synonymous_variant
Transcription ID ENST00000053867
Start 44349539:44349539(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.252C>T
Mutation Classification Silent
Feature Type Transcript