Primary Site >> Pancreatic Cancer

Gene >> CHL1

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000397491
Start 366046:366046(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1634A>G
AA Mutation p.Lys545Arg(p.K545R)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence synonymous_variant
Transcription ID ENST00000397491
Start 391685:391685(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs140090602
CDS Mutation c.2754G>A
Mutation Classification Silent
Feature Type Transcript
ID 3
Mutation Consequence synonymous_variant
Transcription ID ENST00000397491
Start 398237:398237(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs373156471
CDS Mutation c.3057C>T
Mutation Classification Silent
Feature Type Transcript
ID 4
Mutation Consequence stop_gained
Transcription ID ENST00000397491
Start 391790:391790(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2859T>A
AA Mutation p.Tyr953Ter(p.Y953*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript