Primary Site >> Pancreatic Cancer

Gene >> TNFRSF19

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000382258
Start 23626787:23626787(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs368876279
CDS Mutation c.440C>T
AA Mutation p.Pro147Leu(p.P147L)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000382258
Start 23626784:23626784(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs747142846
CDS Mutation c.437A>C
AA Mutation p.Glu146Ala(p.E146A)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence synonymous_variant
Transcription ID ENST00000382258
Start 23668809:23668809(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.957C>T
Mutation Classification Silent
Feature Type Transcript
ID 4
Mutation Consequence synonymous_variant
Transcription ID ENST00000382258
Start 23615971:23615971(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs762063764
CDS Mutation c.285C>T
Mutation Classification Silent
Feature Type Transcript
ID 5
Mutation Consequence stop_gained
Transcription ID ENST00000382258
Start 23669107:23669107(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs201826458
CDS Mutation c.1255C>T
AA Mutation p.Arg419Ter(p.R419*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript