Primary Site >> Stomach Cancer
Gene >> CEL
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000372080 |
| Start | 133071040:133071040(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs762461399 |
| CDS Mutation | c.1547C>T |
| AA Mutation | p.Thr516Met(p.T516M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000372080 |
| Start | 133071741:133071741(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2248A>G |
| AA Mutation | p.Met750Val(p.M750V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000372080 |
| Start | 133070556:133070556(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1391A>G |
| AA Mutation | p.Tyr464Cys(p.Y464C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000372080 |
| Start | 133064410:133064410(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs779607772 |
| CDS Mutation | c.82G>A |
| AA Mutation | p.Ala28Thr(p.A28T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000372080 |
| Start | 133071748:133071748(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2255C>T |
| AA Mutation | p.Ala752Val(p.A752V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000372080 |
| Start | 133064540:133064540(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.212A>G |
| AA Mutation | p.His71Arg(p.H71R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000372080 |
| Start | 133066863:133066863(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.704T>C |
| AA Mutation | p.Leu235Pro(p.L235P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000372080 |
| Start | 133064674:133064674(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.261C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000372080 |
| Start | 133065080:133065080(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.390C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000372080 |
| Start | 133067108:133067108(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.807C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000372080 |
| Start | 133066595:133066595(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | rs769282739 |
| CDS Mutation | c.619delG |
| AA Mutation | p.Asp207ThrfsTer41(p.D207Tfs*41) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |