Primary Site >> Stomach Cancer
Gene >> EZH2
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000460911 |
| Start | 148846588:148846588(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.128G>T |
| AA Mutation | p.Ser43Ile(p.S43I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000460911 |
| Start | 148807669:148807669(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs397515548 |
| CDS Mutation | c.2218G>A |
| AA Mutation | p.Glu740Lys(p.E740K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000460911 |
| Start | 148813972:148813972(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs561605379 |
| CDS Mutation | c.1823G>A |
| AA Mutation | p.Arg608Gln(p.R608Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000460911 |
| Start | 148810362:148810362(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1985T>C |
| AA Mutation | p.Met662Thr(p.M662T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000460911 |
| Start | 148847247:148847247(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs771352080 |
| CDS Mutation | c.52C>T |
| AA Mutation | p.Arg18Cys(p.R18C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000460911 |
| Start | 148847236:148847236(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.63A>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000460911 |
| Start | 148809118:148809118(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.2133delT |
| AA Mutation | p.Phe711LeufsTer24(p.F711Lfs*24) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |