Primary Site >> Liver Cancer
Gene >> TET1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000373644 |
| Start | 68686674:68686674(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.5371A>T |
| AA Mutation | p.Asn1791Tyr(p.N1791Y) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000373644 |
| Start | 68690963:68690963(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.5560A>G |
| AA Mutation | p.Thr1854Ala(p.T1854A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000373644 |
| Start | 68572768:68572768(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.430A>G |
| AA Mutation | p.Ile144Val(p.I144V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000373644 |
| Start | 68574157:68574157(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1819A>G |
| AA Mutation | p.Thr607Ala(p.T607A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000373644 |
| Start | 68572790:68572790(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.452A>G |
| AA Mutation | p.Lys151Arg(p.K151R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000373644 |
| Start | 68646484:68646484(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3755A>T |
| AA Mutation | p.Glu1252Val(p.E1252V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000373644 |
| Start | 68667195:68667195(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.4612A>C |
| AA Mutation | p.Thr1538Pro(p.T1538P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000373644 |
| Start | 68645370:68645370(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs764721765 |
| CDS Mutation | c.2641A>G |
| AA Mutation | p.Met881Val(p.M881V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |