Primary Site >> Stomach Cancer
Gene >> CDK20
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000325303 |
| Start | 87974395:87974395(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.52G>T |
| AA Mutation | p.Val18Phe(p.V18F) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000325303 |
| Start | 87969830:87969830(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs150288403 |
| CDS Mutation | c.653G>A |
| AA Mutation | p.Arg218His(p.R218H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000325303 |
| Start | 87969205:87969205(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs542111446 |
| CDS Mutation | c.832G>A |
| AA Mutation | p.Ala278Thr(p.A278T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000325303 |
| Start | 87970579:87970579(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs754174793 |
| CDS Mutation | c.552C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000325303 |
| Start | 87974402:87974402(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.45C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000325303 |
| Start | 87974429:87974429(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.18C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000325303 |
| Start | 87970811:87970811(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs371154514 |
| CDS Mutation | c.465C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000325303 |
| Start | 87973942:87973942(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.169G>T |
| AA Mutation | p.Glu57Ter(p.E57*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000325303 |
| Start | 87970623:87970623(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs773980056 |
| CDS Mutation | c.508C>T |
| AA Mutation | p.Arg170Ter(p.R170*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |