Primary Site >> Liver Cancer

Gene >> NCOR1

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000268712
Start 16137328:16137328(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1492C>T
AA Mutation p.Arg498Cys(p.R498C)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000268712
Start 16061732:16061732(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.5550A>T
AA Mutation p.Glu1850Asp(p.E1850D)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000268712
Start 16139162:16139162(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1198C>T
AA Mutation p.Leu400Phe(p.L400F)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence frameshift_variant
Transcription ID ENST00000268712
Start 16067913:16067913(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.4722delT
AA Mutation p.His1575ThrfsTer40(p.H1575Tfs*40)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 5
Mutation Consequence stop_gained
Transcription ID ENST00000268712
Start 16073522:16073522(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.3718G>T
AA Mutation p.Glu1240Ter(p.E1240*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence frameshift_variant
Transcription ID ENST00000268712
Start 16126142:16126143(version: GRCh38)
Mutation Type INS
dbSNP_RS null
CDS Mutation c.1573dupA
AA Mutation p.Thr525AsnfsTer11(p.T525Nfs*11)
Mutation Classification Frame_Shift_Ins
Feature Type Transcript
ID 7
Mutation Consequence inframe_deletion
Transcription ID ENST00000268712
Start 16039580:16039609(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.6779_6808delATCTTGGGCTGGAAGACATTATCAGGAAGG
AA Mutation p.Asn2260_Ala2270delinsThr(p.N2260_A2270delinsT)
Mutation Classification In_Frame_Del
Feature Type Transcript