Primary Site >> Pancreatic Cancer

Gene >> IRS4

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000372129
Start 108736190:108736190(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.155G>C
AA Mutation p.Gly52Ala(p.G52A)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000372129
Start 108734870:108734870(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1475A>T
AA Mutation p.Asn492Ile(p.N492I)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence synonymous_variant
Transcription ID ENST00000372129
Start 108735874:108735874(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs767408539
CDS Mutation c.471C>T
Mutation Classification Silent
Feature Type Transcript
ID 4
Mutation Consequence synonymous_variant
Transcription ID ENST00000372129
Start 108736057:108736057(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.288C>T
Mutation Classification Silent
Feature Type Transcript
ID 5
Mutation Consequence stop_gained
Transcription ID ENST00000372129
Start 108734523:108734523(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1822A>T
AA Mutation p.Lys608Ter(p.K608*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript