Primary Site >> Pancreatic Cancer

Gene >> HRNR

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000368801
Start 152219662:152219662(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1967C>A
AA Mutation p.Ser656Tyr(p.S656Y)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000368801
Start 152219731:152219731(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1898C>T
AA Mutation p.Ser633Phe(p.S633F)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence synonymous_variant
Transcription ID ENST00000368801
Start 152214621:152214621(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.7008T>A
Mutation Classification Silent
Feature Type Transcript
ID 4
Mutation Consequence synonymous_variant
Transcription ID ENST00000368801
Start 152220354:152220354(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1275C>T
Mutation Classification Silent
Feature Type Transcript
ID 5
Mutation Consequence synonymous_variant
Transcription ID ENST00000368801
Start 152214435:152214435(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.7194T>A
Mutation Classification Silent
Feature Type Transcript