Primary Site >> Pancreatic Cancer

Gene >> POTEF

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000357462
Start 130120160:130120160(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.356C>T
AA Mutation p.Ala119Val(p.A119V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence synonymous_variant
Transcription ID ENST00000357462
Start 130120300:130120300(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.216C>T
Mutation Classification Silent
Feature Type Transcript