Primary Site >> Liver Cancer

Gene >> SIN3B

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000379803
Start 16877583:16877583(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2994G>C
AA Mutation p.Glu998Asp(p.E998D)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence synonymous_variant
Transcription ID ENST00000379803
Start 16862898:16862898(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1281A>C
Mutation Classification Silent
Feature Type Transcript
ID 3
Mutation Consequence synonymous_variant
Transcription ID ENST00000379803
Start 16841788:16841788(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.402G>C
Mutation Classification Silent
Feature Type Transcript
ID 4
Mutation Consequence inframe_insertion
Transcription ID ENST00000379803
Start 16878544:16878545(version: GRCh38)
Mutation Type INS
dbSNP_RS novel
CDS Mutation c.3307_3308insGTC
AA Mutation p.Trp1102_His1103insArg(p.W1102_H1103insR)
Mutation Classification In_Frame_Ins
Feature Type Transcript
ID 5
Mutation Consequence inframe_insertion
Transcription ID ENST00000379803
Start 16878546:16878547(version: GRCh38)
Mutation Type INS
dbSNP_RS novel
CDS Mutation c.3308_3309insTAGCTGTTTCCTGAG
AA Mutation p.Ser1104_Arg1105insCysPheLeuSerSer(p.S1104_R1105insCFLSS)
Mutation Classification In_Frame_Ins
Feature Type Transcript