Primary Site >> Stomach Cancer
Gene >> CDT1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000301019 |
| Start | 88805794:88805794(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs143284523 |
| CDS Mutation | c.757C>T |
| AA Mutation | p.Arg253Cys(p.R253C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000301019 |
| Start | 88805618:88805618(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs373340835 |
| CDS Mutation | c.667G>A |
| AA Mutation | p.Val223Ile(p.V223I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000301019 |
| Start | 88805448:88805448(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.497A>C |
| AA Mutation | p.Lys166Thr(p.K166T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000301019 |
| Start | 88808195:88808195(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1558T>C |
| AA Mutation | p.Tyr520His(p.Y520H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000301019 |
| Start | 88807383:88807383(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs528610361 |
| CDS Mutation | c.1378G>A |
| AA Mutation | p.Val460Met(p.V460M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000301019 |
| Start | 88805589:88805589(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs146872515 |
| CDS Mutation | c.638C>T |
| AA Mutation | p.Thr213Met(p.T213M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000301019 |
| Start | 88808181:88808181(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1544T>C |
| AA Mutation | p.Ile515Thr(p.I515T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000301019 |
| Start | 88807421:88807421(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1416G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000301019 |
| Start | 88805820:88805820(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.783C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000301019 |
| Start | 88805455:88805455(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs534417526 |
| CDS Mutation | c.504C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |