Primary Site >> Liver Cancer
Gene >> CUL9
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000252050 |
| Start | 43222858:43222858(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.7112A>G |
| AA Mutation | p.Asn2371Ser(p.N2371S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000252050 |
| Start | 43206502:43206502(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.5204A>G |
| AA Mutation | p.Tyr1735Cys(p.Y1735C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000252050 |
| Start | 43193083:43193083(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2263C>T |
| AA Mutation | p.Leu755Phe(p.L755F) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000252050 |
| Start | 43185528:43185528(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.668G>A |
| AA Mutation | p.Arg223His(p.R223H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000252050 |
| Start | 43215088:43215088(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.5698G>T |
| AA Mutation | p.Ala1900Ser(p.A1900S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000252050 |
| Start | 43215089:43215089(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs146106470 |
| CDS Mutation | c.5699C>T |
| AA Mutation | p.Ala1900Val(p.A1900V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000252050 |
| Start | 43205002:43205002(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.4519C>G |
| AA Mutation | p.His1507Asp(p.H1507D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000252050 |
| Start | 43187363:43187363(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1505T>C |
| AA Mutation | p.Leu502Pro(p.L502P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000252050 |
| Start | 43213564:43213564(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs747458428 |
| CDS Mutation | c.5485G>A |
| AA Mutation | p.Gly1829Arg(p.G1829R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000252050 |
| Start | 43187269:43187269(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1411C>T |
| AA Mutation | p.Pro471Ser(p.P471S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000252050 |
| Start | 43187271:43187271(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1413T>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000252050 |
| Start | 43198736:43198736(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2931C>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000252050 |
| Start | 43193202:43193202(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs775629593 |
| CDS Mutation | c.2382G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000252050 |
| Start | 43224262:43224262(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.7371C>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000252050 |
| Start | 43213281:43213284(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.5348_5351delATCA |
| AA Mutation | p.Asn1783ArgfsTer7(p.N1783Rfs*7) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | splice_acceptor_variant |
| Transcription ID | ENST00000252050 |
| Start | 43204746:43204746(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.4340-2A>C |
| Mutation Classification | Splice_Site |
| Feature Type | Transcript |