Primary Site >> Stomach Cancer
Gene >> RIOK1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000379834 |
| Start | 7404482:7404482(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.919G>A |
| AA Mutation | p.Val307Ile(p.V307I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000379834 |
| Start | 7405253:7405253(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1101C>A |
| AA Mutation | p.Phe367Leu(p.F367L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000379834 |
| Start | 7414389:7414389(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1595A>C |
| AA Mutation | p.Lys532Thr(p.K532T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000379834 |
| Start | 7411367:7411367(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1305T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000379834 |
| Start | 7393258:7393258(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.231A>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000379834 |
| Start | 7405014:7405014(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs759988992 |
| CDS Mutation | c.1089C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | inframe_insertion |
| Transcription ID | ENST00000379834 |
| Start | 7393214:7393215(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | rs764932797 |
| CDS Mutation | c.189_191dupTGA |
| AA Mutation | p.Asp69dup(p.D69dup) |
| Mutation Classification | In_Frame_Ins |
| Feature Type | Transcript |