Primary Site >> Stomach Cancer
Gene >> SPG7
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000268704 |
| Start | 89548050:89548050(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs753722512 |
| CDS Mutation | c.1600C>T |
| AA Mutation | p.Arg534Trp(p.R534W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000268704 |
| Start | 89544746:89544746(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs765608610 |
| CDS Mutation | c.1423G>A |
| AA Mutation | p.Val475Ile(p.V475I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000268704 |
| Start | 89548092:89548092(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs771640502 |
| CDS Mutation | c.1642G>A |
| AA Mutation | p.Ala548Thr(p.A548T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000268704 |
| Start | 89526429:89526429(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.719G>T |
| AA Mutation | p.Arg240Met(p.R240M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000268704 |
| Start | 89548075:89548075(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1625C>T |
| AA Mutation | p.Thr542Ile(p.T542I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000268704 |
| Start | 89532525:89532525(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs115999025 |
| CDS Mutation | c.1213G>A |
| AA Mutation | p.Val405Ile(p.V405I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000268704 |
| Start | 89556980:89556980(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs140769107 |
| CDS Mutation | c.2275G>A |
| AA Mutation | p.Ala759Thr(p.A759T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000268704 |
| Start | 89556891:89556891(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2186C>T |
| AA Mutation | p.Ala729Val(p.A729V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000268704 |
| Start | 89553871:89553871(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs369503365 |
| CDS Mutation | c.2014G>A |
| AA Mutation | p.Gly672Arg(p.G672R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000268704 |
| Start | 89524031:89524031(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.402C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000268704 |
| Start | 89526454:89526454(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs200603189 |
| CDS Mutation | c.744A>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000268704 |
| Start | 89532050:89532050(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs762445020 |
| CDS Mutation | c.1134C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000268704 |
| Start | 89532478:89532478(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.1166delG |
| AA Mutation | p.Arg389LeufsTer50(p.R389Lfs*50) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000268704 |
| Start | 89550502:89550502(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.1676delA |
| AA Mutation | p.Lys559ArgfsTer33(p.K559Rfs*33) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |