Primary Site >> Liver Cancer
Gene >> SPAG17
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000336338 |
| Start | 118086893:118086893(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1475G>T |
| AA Mutation | p.Cys492Phe(p.C492F) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000336338 |
| Start | 118016050:118016050(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.4202A>C |
| AA Mutation | p.Asn1401Thr(p.N1401T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000336338 |
| Start | 118097818:118097818(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.863C>T |
| AA Mutation | p.Ala288Val(p.A288V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000336338 |
| Start | 117992548:117992548(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.5279C>T |
| AA Mutation | p.Pro1760Leu(p.P1760L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000336338 |
| Start | 118005478:118005478(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.4712A>T |
| AA Mutation | p.Tyr1571Phe(p.Y1571F) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000336338 |
| Start | 118093217:118093217(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1112T>A |
| AA Mutation | p.Leu371His(p.L371H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000336338 |
| Start | 118016173:118016173(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.4079A>C |
| AA Mutation | p.His1360Pro(p.H1360P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000336338 |
| Start | 118031808:118031808(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3493G>T |
| AA Mutation | p.Val1165Leu(p.V1165L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000336338 |
| Start | 118081162:118081162(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs772450473 |
| CDS Mutation | c.2148T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000336338 |
| Start | 118042028:118042028(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2829G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000336338 |
| Start | 117996631:117996631(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.4889delA |
| AA Mutation | p.Asn1630IlefsTer31(p.N1630Ifs*31) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000336338 |
| Start | 117996494:117996494(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.4929delT |
| AA Mutation | p.Phe1643LeufsTer18(p.F1643Lfs*18) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |