Primary Site >> Pancreatic Cancer

Gene >> RRAD

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000299759
Start 66922187:66922187(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.816G>T
AA Mutation p.Glu272Asp(p.E272D)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence synonymous_variant
Transcription ID ENST00000299759
Start 66922277:66922277(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.726G>T
Mutation Classification Silent
Feature Type Transcript