Primary Site >> Pancreatic Cancer

Gene >> PDGFRB

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000261799
Start 150133963:150133963(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.677G>A
AA Mutation p.Arg226His(p.R226H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000261799
Start 150120965:150120965(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2509G>T
AA Mutation p.Gly837Cys(p.G837C)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence synonymous_variant
Transcription ID ENST00000261799
Start 150115850:150115850(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.3234C>A
Mutation Classification Silent
Feature Type Transcript
ID 4
Mutation Consequence synonymous_variant
Transcription ID ENST00000261799
Start 150132922:150132922(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.955C>T
Mutation Classification Silent
Feature Type Transcript