Primary Site >> Esophagus Cancer

Gene >> PRMT1

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000454376
Start 49682007:49682007(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs750309006
CDS Mutation c.290C>T
AA Mutation p.Ser97Leu(p.S97L)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000454376
Start 49677288:49677288(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.8C>T
AA Mutation p.Ala3Val(p.A3V)
Mutation Classification Missense_Mutation
Feature Type Transcript