Primary Site >> Stomach Cancer
Gene >> OPRD1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000234961 |
| Start | 28858989:28858989(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.263T>C |
| AA Mutation | p.Ile88Thr(p.I88T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000234961 |
| Start | 28862945:28862945(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.781C>T |
| AA Mutation | p.Arg261Cys(p.R261C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000234961 |
| Start | 28862757:28862757(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.593G>A |
| AA Mutation | p.Cys198Tyr(p.C198Y) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000234961 |
| Start | 28863153:28863153(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.989G>A |
| AA Mutation | p.Arg330His(p.R330H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000234961 |
| Start | 28859162:28859162(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs778293667 |
| CDS Mutation | c.436C>T |
| AA Mutation | p.Arg146Cys(p.R146C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000234961 |
| Start | 28862983:28862983(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs142127727 |
| CDS Mutation | c.819T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |