Primary Site >> Liver Cancer
Gene >> TET2
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000380013 |
| Start | 105243576:105243576(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3601C>T |
| AA Mutation | p.Arg1201Cys(p.R1201C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000380013 |
| Start | 105234448:105234448(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.506A>T |
| AA Mutation | p.His169Leu(p.H169L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000380013 |
| Start | 105236534:105236534(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2592C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000380013 |
| Start | 105237176:105237176(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs184727510 |
| CDS Mutation | c.3234C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000380013 |
| Start | 105234010:105234011(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | novel |
| CDS Mutation | c.68_69insT |
| AA Mutation | p.Ile24HisfsTer19(p.I24Hfs*19) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000380013 |
| Start | 105234011:105234012(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | novel |
| CDS Mutation | c.69_70insCA |
| AA Mutation | p.Ile24GlnfsTer26(p.I24Qfs*26) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |