Primary Site >> Pancreatic Cancer

Gene >> IRF8

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000268638
Start 85918584:85918584(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs751576714
CDS Mutation c.769G>A
AA Mutation p.Ala257Thr(p.A257T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000268638
Start 85921212:85921212(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs772557507
CDS Mutation c.1211G>A
AA Mutation p.Arg404Gln(p.R404Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000268638
Start 85918644:85918644(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.829G>A
AA Mutation p.Gly277Arg(p.G277R)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence synonymous_variant
Transcription ID ENST00000268638
Start 85909127:85909127(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs541779534
CDS Mutation c.312C>T
Mutation Classification Silent
Feature Type Transcript