Primary Site >> Stomach Cancer
Gene >> PLK4
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000270861 |
| Start | 127883465:127883465(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.249T>G |
| AA Mutation | p.Asn83Lys(p.N83K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000270861 |
| Start | 127881892:127881892(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.92C>T |
| AA Mutation | p.Ser31Phe(p.S31F) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000270861 |
| Start | 127887425:127887425(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1388C>T |
| AA Mutation | p.Pro463Leu(p.P463L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000270861 |
| Start | 127894955:127894955(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2565G>T |
| AA Mutation | p.Met855Ile(p.M855I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000270861 |
| Start | 127886491:127886491(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs374708135 |
| CDS Mutation | c.1121G>A |
| AA Mutation | p.Arg374His(p.R374H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000270861 |
| Start | 127893853:127893853(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2534C>T |
| AA Mutation | p.Pro845Leu(p.P845L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000270861 |
| Start | 127893545:127893545(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2355A>G |
| AA Mutation | p.Ile785Met(p.I785M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000270861 |
| Start | 127886003:127886003(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs761455609 |
| CDS Mutation | c.633C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |