Primary Site >> Liver Cancer
Gene >> NCOR2
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000405201 |
| Start | 124337151:124337151(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.5717C>T |
| AA Mutation | p.Pro1906Leu(p.P1906L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000405201 |
| Start | 124350722:124350722(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs755508738 |
| CDS Mutation | c.3709G>A |
| AA Mutation | p.Val1237Ile(p.V1237I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000405201 |
| Start | 124350670:124350670(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3761G>A |
| AA Mutation | p.Arg1254His(p.R1254H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000405201 |
| Start | 124402449:124402449(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1595A>T |
| AA Mutation | p.Glu532Val(p.E532V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000405201 |
| Start | 124344798:124344798(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.4513G>A |
| AA Mutation | p.Glu1505Lys(p.E1505K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000405201 |
| Start | 124340407:124340407(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs773108865 |
| CDS Mutation | c.5375C>T |
| AA Mutation | p.Ser1792Phe(p.S1792F) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000405201 |
| Start | 124354921:124354921(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3400C>T |
| AA Mutation | p.His1134Tyr(p.H1134Y) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000405201 |
| Start | 124430644:124430644(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1026G>T |
| AA Mutation | p.Lys342Asn(p.K342N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000405201 |
| Start | 124398154:124398154(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1841G>A |
| AA Mutation | p.Arg614His(p.R614H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000405201 |
| Start | 124346615:124346615(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs779461576 |
| CDS Mutation | c.4308G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000405201 |
| Start | 124340325:124340325(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs780246024 |
| CDS Mutation | c.5457G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000405201 |
| Start | 124350615:124350616(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | novel |
| CDS Mutation | c.3815dupG |
| AA Mutation | p.Lys1273GlnfsTer9(p.K1273Qfs*9) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | splice_acceptor_variant;coding_sequence_variant;intron_variant |
| Transcription ID | ENST00000405201 |
| Start | 124337173:124337207(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.5688-27_5695delGCCTGACCGCCTTCTCTCCTCCCCCAGGTCCACCT |
| Mutation Classification | Splice_Site |
| Feature Type | Transcript |