Primary Site >> Pancreatic Cancer

Gene >> NRCAM

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000379028
Start 108226288:108226288(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.641A>G
AA Mutation p.Glu214Gly(p.E214G)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000379028
Start 108184585:108184585(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2065C>A
AA Mutation p.His689Asn(p.H689N)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence synonymous_variant
Transcription ID ENST00000379028
Start 108150069:108150069(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs771749042
CDS Mutation c.3756C>T
Mutation Classification Silent
Feature Type Transcript
ID 4
Mutation Consequence synonymous_variant
Transcription ID ENST00000379028
Start 108191258:108191258(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1929T>G
Mutation Classification Silent
Feature Type Transcript