Primary Site >> Stomach Cancer
Gene >> CSNK1A1L
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000379800 |
| Start | 37104872:37104872(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.385A>G |
| AA Mutation | p.Thr129Ala(p.T129A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000379800 |
| Start | 37105223:37105223(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs759647226 |
| CDS Mutation | c.34G>A |
| AA Mutation | p.Val12Ile(p.V12I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000379800 |
| Start | 37105074:37105074(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.183C>A |
| AA Mutation | p.Ser61Arg(p.S61R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000379800 |
| Start | 37105187:37105187(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.70G>A |
| AA Mutation | p.Gly24Arg(p.G24R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000379800 |
| Start | 37104697:37104697(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.560A>G |
| AA Mutation | p.Tyr187Cys(p.Y187C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000379800 |
| Start | 37104718:37104718(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.539A>G |
| AA Mutation | p.His180Arg(p.H180R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000379800 |
| Start | 37105041:37105041(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.216C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000379800 |
| Start | 37105167:37105167(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs369173905 |
| CDS Mutation | c.90C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000379800 |
| Start | 37105008:37105008(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.249delA |
| AA Mutation | p.Asp84ThrfsTer5(p.D84Tfs*5) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |