Primary Site >> Stomach Cancer
Gene >> SRMS
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000217188 |
| Start | 63542265:63542265(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs751298544 |
| CDS Mutation | c.844C>T |
| AA Mutation | p.His282Tyr(p.H282Y) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000217188 |
| Start | 63540870:63540870(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1415C>G |
| AA Mutation | p.Ser472Cys(p.S472C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000217188 |
| Start | 63547123:63547123(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs373892181 |
| CDS Mutation | c.341C>T |
| AA Mutation | p.Thr114Met(p.T114M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000217188 |
| Start | 63543363:63543363(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.596C>T |
| AA Mutation | p.Ala199Val(p.A199V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000217188 |
| Start | 63540947:63540947(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs764818396 |
| CDS Mutation | c.1338G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000217188 |
| Start | 63547398:63547398(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs768842767 |
| CDS Mutation | c.66G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |