Primary Site >> Liver Cancer

Gene >> BRD4

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000263377
Start 15257146:15257146(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1369A>T
AA Mutation p.Met457Leu(p.M457L)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000263377
Start 15244384:15244384(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2428C>T
AA Mutation p.Pro810Ser(p.P810S)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000263377
Start 15265601:15265601(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.602A>C
AA Mutation p.Gln201Pro(p.Q201P)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000263377
Start 15239951:15239951(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3241C>T
AA Mutation p.His1081Tyr(p.H1081Y)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000263377
Start 15239817:15239817(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.3287T>C
AA Mutation p.Leu1096Pro(p.L1096P)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence frameshift_variant
Transcription ID ENST00000263377
Start 15244302:15244314(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.2498_2510delCTGAGCTGCCCCC
AA Mutation p.Pro833LeufsTer58(p.P833Lfs*58)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 7
Mutation Consequence stop_gained
Transcription ID ENST00000263377
Start 15238769:15238769(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3994G>T
AA Mutation p.Glu1332Ter(p.E1332*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript