Primary Site >> Liver Cancer
Gene >> CASP8AP2
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000551025 |
| Start | 89862997:89862997(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1288G>T |
| AA Mutation | p.Asp430Tyr(p.D430Y) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000551025 |
| Start | 89867954:89867954(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.4664G>A |
| AA Mutation | p.Gly1555Asp(p.G1555D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000551025 |
| Start | 89863713:89863713(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2004G>T |
| AA Mutation | p.Met668Ile(p.M668I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000551025 |
| Start | 89853188:89853188(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.78T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000551025 |
| Start | 89871298:89871298(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.5802C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000551025 |
| Start | 89862738:89862738(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs9444715 |
| CDS Mutation | c.1029A>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000551025 |
| Start | 89862200:89862218(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.493_511delAAATCTAGATCTCCACATT |
| AA Mutation | p.Lys165TrpfsTer96(p.K165Wfs*96) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |