Primary Site >> Stomach Cancer
Gene >> OMP
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000529803 |
| Start | 77103129:77103129(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs375214001 |
| CDS Mutation | c.290G>A |
| AA Mutation | p.Arg97His(p.R97H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000529803 |
| Start | 77102955:77102955(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs369608660 |
| CDS Mutation | c.116G>A |
| AA Mutation | p.Arg39His(p.R39H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000529803 |
| Start | 77103141:77103141(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.302A>G |
| AA Mutation | p.Asp101Gly(p.D101G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000529803 |
| Start | 77103050:77103050(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs782325915 |
| CDS Mutation | c.211G>A |
| AA Mutation | p.Val71Met(p.V71M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000529803 |
| Start | 77102924:77102924(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs375866081 |
| CDS Mutation | c.85G>A |
| AA Mutation | p.Val29Met(p.V29M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000529803 |
| Start | 77103035:77103035(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs782214575 |
| CDS Mutation | c.196G>A |
| AA Mutation | p.Glu66Lys(p.E66K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000529803 |
| Start | 77103079:77103079(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.240C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000529803 |
| Start | 77102881:77102881(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs376088397 |
| CDS Mutation | c.42G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |