Primary Site >> Stomach Cancer
Gene >> RAF1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000251849 |
| Start | 12604200:12604200(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs80338796 |
| CDS Mutation | c.770C>T |
| AA Mutation | p.Ser257Leu(p.S257L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000251849 |
| Start | 12599750:12599750(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1049T>C |
| AA Mutation | p.Met350Thr(p.M350T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000251849 |
| Start | 12584581:12584581(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs730881006 |
| CDS Mutation | c.1880G>A |
| AA Mutation | p.Arg627Gln(p.R627Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000251849 |
| Start | 12584603:12584603(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1858G>A |
| AA Mutation | p.Ala620Thr(p.A620T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000251849 |
| Start | 12600187:12600187(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs749989518 |
| CDS Mutation | c.955G>A |
| AA Mutation | p.Ala319Thr(p.A319T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000251849 |
| Start | 12606213:12606213(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.668G>T |
| AA Mutation | p.Arg223Met(p.R223M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000251849 |
| Start | 12591708:12591708(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs730880382 |
| CDS Mutation | c.1193G>T |
| AA Mutation | p.Arg398Leu(p.R398L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000251849 |
| Start | 12590929:12590929(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1239A>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000251849 |
| Start | 12618692:12618692(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs140806518 |
| CDS Mutation | c.30G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |