Primary Site >> Pancreatic Cancer

Gene >> PIAS4

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000262971
Start 4033505:4033505(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1067T>C
AA Mutation p.Met356Thr(p.M356T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant;splice_region_variant
Transcription ID ENST00000262971
Start 4033579:4033579(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1141G>A
AA Mutation p.Gly381Arg(p.G381R)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence synonymous_variant
Transcription ID ENST00000262971
Start 4028842:4028842(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs148838008
CDS Mutation c.795C>T
Mutation Classification Silent
Feature Type Transcript
ID 4
Mutation Consequence synonymous_variant
Transcription ID ENST00000262971
Start 4037770:4037770(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs746927508
CDS Mutation c.1428G>A
Mutation Classification Silent
Feature Type Transcript