Primary Site >> Pancreatic Cancer

Gene >> CHEK2

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000328354
Start 28734554:28734554(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.168C>G
AA Mutation p.Ser56Arg(p.S56R)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence synonymous_variant
Transcription ID ENST00000328354
Start 28694065:28694065(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1428G>A
Mutation Classification Silent
Feature Type Transcript