Primary Site >> Stomach Cancer
Gene >> FAP
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000188790 |
| Start | 162198790:162198790(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs780875561 |
| CDS Mutation | c.1369G>A |
| AA Mutation | p.Asp457Asn(p.D457N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000188790 |
| Start | 162242919:162242919(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs145562225 |
| CDS Mutation | c.80G>A |
| AA Mutation | p.Arg27His(p.R27H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000188790 |
| Start | 162218139:162218139(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.609G>T |
| AA Mutation | p.Glu203Asp(p.E203D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000188790 |
| Start | 162198784:162198784(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs751170815 |
| CDS Mutation | c.1375G>A |
| AA Mutation | p.Ala459Thr(p.A459T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000188790 |
| Start | 162215976:162215976(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs769751511 |
| CDS Mutation | c.788G>A |
| AA Mutation | p.Arg263Gln(p.R263Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000188790 |
| Start | 162213993:162213993(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs756858958 |
| CDS Mutation | c.947C>T |
| AA Mutation | p.Ser316Leu(p.S316L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000188790 |
| Start | 162173191:162173191(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2065T>A |
| AA Mutation | p.Phe689Ile(p.F689I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000188790 |
| Start | 162173725:162173725(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2032A>G |
| AA Mutation | p.Lys678Glu(p.K678E) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000188790 |
| Start | 162174943:162174943(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs765141629 |
| CDS Mutation | c.1893A>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000188790 |
| Start | 162200571:162200571(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs767070470 |
| CDS Mutation | c.1272C>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000188790 |
| Start | 162200589:162200589(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs763694305 |
| CDS Mutation | c.1254C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |