Primary Site >> Stomach Cancer
Gene >> PLK2
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000274289 |
| Start | 58456975:58456975(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1126A>C |
| AA Mutation | p.Lys376Gln(p.K376Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000274289 |
| Start | 58459067:58459067(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.296T>C |
| AA Mutation | p.Met99Thr(p.M99T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000274289 |
| Start | 58456951:58456951(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1150A>T |
| AA Mutation | p.Thr384Ser(p.T384S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000274289 |
| Start | 58456544:58456544(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1202A>T |
| AA Mutation | p.Asp401Val(p.D401V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000274289 |
| Start | 58456524:58456524(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1222A>C |
| AA Mutation | p.Thr408Pro(p.T408P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000274289 |
| Start | 58457570:58457570(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.727A>G |
| AA Mutation | p.Thr243Ala(p.T243A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000274289 |
| Start | 58458777:58458777(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs779187630 |
| CDS Mutation | c.443A>G |
| AA Mutation | p.Tyr148Cys(p.Y148C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000274289 |
| Start | 58459944:58459944(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.16A>G |
| AA Mutation | p.Thr6Ala(p.T6A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000274289 |
| Start | 58455694:58455694(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1470T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000274289 |
| Start | 58459855:58459855(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.105G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000274289 |
| Start | 58459939:58459939(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.21C>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000274289 |
| Start | 58457185:58457185(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | rs772701630 |
| CDS Mutation | c.1004delT |
| AA Mutation | p.Leu335CysfsTer68(p.L335Cfs*68) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |