Primary Site >> Stomach Cancer
Gene >> OSM
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000215781 |
| Start | 30264425:30264425(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.217C>T |
| AA Mutation | p.His73Tyr(p.H73Y) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000215781 |
| Start | 30265073:30265073(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs551223066 |
| CDS Mutation | c.106C>T |
| AA Mutation | p.Arg36Cys(p.R36C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000215781 |
| Start | 30263990:30263990(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs200749557 |
| CDS Mutation | c.652C>T |
| AA Mutation | p.Arg218Trp(p.R218W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000215781 |
| Start | 30263920:30263920(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.722G>A |
| AA Mutation | p.Gly241Asp(p.G241D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000215781 |
| Start | 30264213:30264213(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs763555458 |
| CDS Mutation | c.429C>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000215781 |
| Start | 30264096:30264096(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs115512471 |
| CDS Mutation | c.546G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |