Primary Site >> Stomach Cancer
Gene >> ELK3
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000228741 |
| Start | 96247675:96247675(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs751599496 |
| CDS Mutation | c.943G>A |
| AA Mutation | p.Ala315Thr(p.A315T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000228741 |
| Start | 96247358:96247358(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs781432909 |
| CDS Mutation | c.626C>T |
| AA Mutation | p.Ala209Val(p.A209V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000228741 |
| Start | 96247365:96247365(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs780839884 |
| CDS Mutation | c.633C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000228741 |
| Start | 96247437:96247437(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs555376474 |
| CDS Mutation | c.705C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000228741 |
| Start | 96247023:96247023(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs200818787 |
| CDS Mutation | c.291G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000228741 |
| Start | 96247074:96247074(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs770276677 |
| CDS Mutation | c.342G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000228741 |
| Start | 96247383:96247383(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs140155479 |
| CDS Mutation | c.651C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000228741 |
| Start | 96247250:96247251(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | rs769175197 |
| CDS Mutation | c.525dupC |
| AA Mutation | p.Val176ArgfsTer14(p.V176Rfs*14) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |