Primary Site >> Pancreatic Cancer

Gene >> BCL11A

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000335712
Start 60461120:60461120(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1792G>T
AA Mutation p.Asp598Tyr(p.D598Y)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence synonymous_variant
Transcription ID ENST00000335712
Start 60461001:60461001(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1911G>A
Mutation Classification Silent
Feature Type Transcript
ID 3
Mutation Consequence synonymous_variant
Transcription ID ENST00000335712
Start 60461460:60461460(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs767991735
CDS Mutation c.1452C>T
Mutation Classification Silent
Feature Type Transcript
ID 4
Mutation Consequence synonymous_variant
Transcription ID ENST00000335712
Start 60461490:60461490(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1422C>T
Mutation Classification Silent
Feature Type Transcript