Primary Site >> Stomach Cancer
Gene >> CDK14
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000380050 |
| Start | 90790629:90790629(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.521C>T |
| AA Mutation | p.Thr174Ile(p.T174I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000380050 |
| Start | 90917706:90917706(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.808T>G |
| AA Mutation | p.Leu270Val(p.L270V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000380050 |
| Start | 91112661:91112661(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs546258215 |
| CDS Mutation | c.1274G>A |
| AA Mutation | p.Arg425Gln(p.R425Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000380050 |
| Start | 90726741:90726741(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.298T>C |
| AA Mutation | p.Cys100Arg(p.C100R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000380050 |
| Start | 90917698:90917698(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs376270298 |
| CDS Mutation | c.800C>T |
| AA Mutation | p.Thr267Met(p.T267M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000380050 |
| Start | 90984215:90984215(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1015C>G |
| AA Mutation | p.Gln339Glu(p.Q339E) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000380050 |
| Start | 90917635:90917635(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.737A>T |
| AA Mutation | p.Tyr246Phe(p.Y246F) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000380050 |
| Start | 91045901:91045901(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1046T>C |
| AA Mutation | p.Leu349Pro(p.L349P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000380050 |
| Start | 90917649:90917649(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.751T>C |
| AA Mutation | p.Tyr251His(p.Y251H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000380050 |
| Start | 91118136:91118136(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1366A>G |
| AA Mutation | p.Lys456Glu(p.K456E) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000380050 |
| Start | 91112614:91112614(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs151182341 |
| CDS Mutation | c.1227G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000380050 |
| Start | 91079455:91079455(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.1133delA |
| AA Mutation | p.Asn378ThrfsTer12(p.N378Tfs*12) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |