Primary Site >> Stomach Cancer
Gene >> DIRAS3
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000370981 |
| Start | 68046747:68046747(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.551C>G |
| AA Mutation | p.Thr184Ser(p.T184S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000370981 |
| Start | 68046655:68046655(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.643A>G |
| AA Mutation | p.Met215Val(p.M215V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000370981 |
| Start | 68046633:68046633(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.665T>A |
| AA Mutation | p.Leu222Gln(p.L222Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000370981 |
| Start | 68047010:68047010(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs190507981 |
| CDS Mutation | c.288C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000370981 |
| Start | 68047175:68047175(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.123G>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000370981 |
| Start | 68046746:68046746(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.552C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000370981 |
| Start | 68046881:68046881(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.417T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000370981 |
| Start | 68046928:68046928(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.370C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000370981 |
| Start | 68047058:68047058(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs768829006 |
| CDS Mutation | c.240C>A |
| AA Mutation | p.Cys80Ter(p.C80*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |