Primary Site >> Pancreatic Cancer

Gene >> NOS2

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000313735
Start 27764046:27764046(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2527C>T
AA Mutation p.Leu843Phe(p.L843F)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000313735
Start 27788895:27788895(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.232C>T
AA Mutation p.Pro78Ser(p.P78S)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence synonymous_variant
Transcription ID ENST00000313735
Start 27781102:27781102(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.798C>A
Mutation Classification Silent
Feature Type Transcript
ID 4
Mutation Consequence synonymous_variant
Transcription ID ENST00000313735
Start 27783070:27783070(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs775527190
CDS Mutation c.504G>A
Mutation Classification Silent
Feature Type Transcript