Primary Site >> Pancreatic Cancer

Gene >> LAMP2

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000200639
Start 120442641:120442641(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.886C>A
AA Mutation p.Leu296Met(p.L296M)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence synonymous_variant
Transcription ID ENST00000200639
Start 120441740:120441740(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1083G>A
Mutation Classification Silent
Feature Type Transcript