Primary Site >> Pancreatic Cancer

Gene >> PBRM1

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000296302
Start 52586526:52586526(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.3286C>T
AA Mutation p.Arg1096Cys(p.R1096C)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000296302
Start 52603674:52603674(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2626C>T
AA Mutation p.Arg876Cys(p.R876C)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000296302
Start 52564105:52564105(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.3820T>G
AA Mutation p.Leu1274Val(p.L1274V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000296302
Start 52617461:52617461(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1619G>C
AA Mutation p.Arg540Thr(p.R540T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence splice_donor_variant
Transcription ID ENST00000296302
Start 52603519:52603519(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2779+2T>C
Mutation Classification Splice_Site
Feature Type Transcript
ID 6
Mutation Consequence splice_acceptor_variant
Transcription ID ENST00000296302
Start 52615457:52615457(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1819-1G>A
Mutation Classification Splice_Site
Feature Type Transcript
ID 7
Mutation Consequence splice_acceptor_variant
Transcription ID ENST00000296302
Start 52576699:52576699(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.3534-1G>A
Mutation Classification Splice_Site
Feature Type Transcript