Primary Site >> Liver Cancer
Gene >> TPTE
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000618007 |
| Start | 10590500:10590500(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1066T>C |
| AA Mutation | p.Ser356Pro(p.S356P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000618007 |
| Start | 10605487:10605487(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1591T>A |
| AA Mutation | p.Phe531Ile(p.F531I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000618007 |
| Start | 10541132:10541132(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.32C>A |
| AA Mutation | p.Ala11Glu(p.A11E) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000618007 |
| Start | 10605529:10605529(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs267606168 |
| CDS Mutation | c.1633G>T |
| AA Mutation | p.Asp545Tyr(p.D545Y) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000618007 |
| Start | 10569491:10569491(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.621T>A |
| AA Mutation | p.His207Gln(p.H207Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000618007 |
| Start | 10578547:10578547(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.969T>G |
| AA Mutation | p.Asn323Lys(p.N323K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000618007 |
| Start | 10543363:10543363(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.154G>A |
| AA Mutation | p.Val52Met(p.V52M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000618007 |
| Start | 10578583:10578583(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs755583335 |
| CDS Mutation | c.1005G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000618007 |
| Start | 10605504:10605504(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1608T>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000618007 |
| Start | 10605503:10605503(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.1611delT |
| AA Mutation | p.Phe537LeufsTer5(p.F537Lfs*5) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000618007 |
| Start | 10595990:10595990(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1179T>A |
| AA Mutation | p.Tyr393Ter(p.Y393*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |