Primary Site >> Stomach Cancer
Gene >> ORM1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000259396 |
| Start | 114324891:114324891(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs1126746 |
| CDS Mutation | c.430G>T |
| AA Mutation | p.Val144Phe(p.V144F) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000259396 |
| Start | 114323711:114323711(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.163T>C |
| AA Mutation | p.Tyr55His(p.Y55H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000259396 |
| Start | 114323700:114323700(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs146832261 |
| CDS Mutation | c.152G>A |
| AA Mutation | p.Arg51Gln(p.R51Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000259396 |
| Start | 114324837:114324837(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.376A>G |
| AA Mutation | p.Lys126Glu(p.K126E) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | splice_donor_variant |
| Transcription ID | ENST00000259396 |
| Start | 114324899:114324899(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.436+2T>C |
| Mutation Classification | Splice_Site |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | splice_acceptor_variant |
| Transcription ID | ENST00000259396 |
| Start | 114324788:114324788(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs112963597 |
| CDS Mutation | c.329-2A>T |
| Mutation Classification | Splice_Site |
| Feature Type | Transcript |