Primary Site >> Pancreatic Cancer

Gene >> TPR

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000367478
Start 186359804:186359804(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs757801260
CDS Mutation c.1384A>G
AA Mutation p.Met462Val(p.M462V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence synonymous_variant
Transcription ID ENST00000367478
Start 186338096:186338096(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.4299A>G
Mutation Classification Silent
Feature Type Transcript
ID 3
Mutation Consequence synonymous_variant
Transcription ID ENST00000367478
Start 186361671:186361671(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.909A>G
Mutation Classification Silent
Feature Type Transcript
ID 4
Mutation Consequence stop_gained
Transcription ID ENST00000367478
Start 186350325:186350325(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2674G>T
AA Mutation p.Glu892Ter(p.E892*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript