Primary Site >> Pancreatic Cancer

Gene >> LOXL2

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000389131
Start 23328433:23328433(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1099C>A
AA Mutation p.Leu367Met(p.L367M)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000389131
Start 23341142:23341142(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs369286803
CDS Mutation c.593G>A
AA Mutation p.Arg198His(p.R198H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence synonymous_variant
Transcription ID ENST00000389131
Start 23298076:23298076(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs775050327
CDS Mutation c.2292C>T
Mutation Classification Silent
Feature Type Transcript
ID 4
Mutation Consequence synonymous_variant
Transcription ID ENST00000389131
Start 23360114:23360114(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.507C>T
Mutation Classification Silent
Feature Type Transcript