Primary Site >> Stomach Cancer
Gene >> OPRM1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000330432 |
| Start | 154091185:154091185(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs11575856 |
| CDS Mutation | c.877G>A |
| AA Mutation | p.Val293Ile(p.V293I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000330432 |
| Start | 154091162:154091162(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.854T>C |
| AA Mutation | p.Leu285Pro(p.L285P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000330432 |
| Start | 154091414:154091414(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1106G>T |
| AA Mutation | p.Arg369Leu(p.R369L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000330432 |
| Start | 154090086:154090086(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs202015908 |
| CDS Mutation | c.551G>A |
| AA Mutation | p.Arg184Gln(p.R184Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000330432 |
| Start | 154039759:154039759(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs201310502 |
| CDS Mutation | c.215C>T |
| AA Mutation | p.Thr72Met(p.T72M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000330432 |
| Start | 154039743:154039743(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs200207721 |
| CDS Mutation | c.199A>G |
| AA Mutation | p.Met67Val(p.M67V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000330432 |
| Start | 154089933:154089933(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.398G>T |
| AA Mutation | p.Gly133Val(p.G133V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000330432 |
| Start | 154039818:154039818(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.274A>G |
| AA Mutation | p.Met92Val(p.M92V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000330432 |
| Start | 154091265:154091265(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.957T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000330432 |
| Start | 154039781:154039781(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs754904430 |
| CDS Mutation | c.237C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |