Primary Site >> Stomach Cancer
Gene >> FRS3
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000259748 |
| Start | 41771386:41771386(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.712G>T |
| AA Mutation | p.Gly238Cys(p.G238C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000259748 |
| Start | 41770876:41770876(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1222G>T |
| AA Mutation | p.Gly408Trp(p.G408W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000259748 |
| Start | 41771353:41771353(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.745G>A |
| AA Mutation | p.Ala249Thr(p.A249T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000259748 |
| Start | 41771177:41771177(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs201584270 |
| CDS Mutation | c.921G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000259748 |
| Start | 41771330:41771330(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.768C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000259748 |
| Start | 41771348:41771348(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs142384930 |
| CDS Mutation | c.750G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000259748 |
| Start | 41771298:41771298(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.800delC |
| AA Mutation | p.Pro267HisfsTer36(p.P267Hfs*36) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000259748 |
| Start | 41771511:41771511(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.587delC |
| AA Mutation | p.Pro196ArgfsTer45(p.P196Rfs*45) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |