Primary Site >> Pancreatic Cancer

Gene >> CUX1

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000292535
Start 101916190:101916190(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.106G>A
AA Mutation p.Glu36Lys(p.E36K)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant;splice_region_variant
Transcription ID ENST00000292535
Start 102227368:102227368(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.3132A>C
AA Mutation p.Glu1044Asp(p.E1044D)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence synonymous_variant
Transcription ID ENST00000292535
Start 102104386:102104386(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.457C>T
Mutation Classification Silent
Feature Type Transcript
ID 4
Mutation Consequence synonymous_variant
Transcription ID ENST00000437600
Start 102273436:102273436(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs200271633
CDS Mutation c.1326C>T
Mutation Classification Silent
Feature Type Transcript
ID 5
Mutation Consequence synonymous_variant
Transcription ID ENST00000437600
Start 102278047:102278047(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1662G>A
Mutation Classification Silent
Feature Type Transcript