Primary Site >> Stomach Cancer
Gene >> OPRL1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000336866 |
| Start | 64092901:64092901(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs777074407 |
| CDS Mutation | c.181G>A |
| AA Mutation | p.Val61Met(p.V61M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000336866 |
| Start | 64092953:64092953(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.233G>T |
| AA Mutation | p.Arg78Met(p.R78M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000336866 |
| Start | 64098591:64098591(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.905G>A |
| AA Mutation | p.Arg302His(p.R302H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000336866 |
| Start | 64098408:64098408(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs753097004 |
| CDS Mutation | c.722G>A |
| AA Mutation | p.Arg241Gln(p.R241Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000336866 |
| Start | 64098404:64098404(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs774683342 |
| CDS Mutation | c.718C>T |
| AA Mutation | p.Arg240Trp(p.R240W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000336866 |
| Start | 64098553:64098553(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.867G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000336866 |
| Start | 64098057:64098057(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs141501506 |
| CDS Mutation | c.489G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000336866 |
| Start | 64098433:64098433(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs770191548 |
| CDS Mutation | c.747G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000336866 |
| Start | 64098373:64098373(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs781489806 |
| CDS Mutation | c.687C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000336866 |
| Start | 64098751:64098751(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs367711919 |
| CDS Mutation | c.1065C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |