Primary Site >> Stomach Cancer
Gene >> TSPAN4
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000397397 |
| Start | 850341:850341(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs763642214 |
| CDS Mutation | c.37A>G |
| AA Mutation | p.Met13Val(p.M13V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000397397 |
| Start | 866596:866596(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.683G>A |
| AA Mutation | p.Cys228Tyr(p.C228Y) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000397397 |
| Start | 865592:865592(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.410C>A |
| AA Mutation | p.Ala137Asp(p.A137D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000397397 |
| Start | 862575:862575(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.89T>G |
| AA Mutation | p.Val30Gly(p.V30G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000397397 |
| Start | 865745:865745(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs539296350 |
| CDS Mutation | c.484G>A |
| AA Mutation | p.Ala162Thr(p.A162T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000397397 |
| Start | 850310:850310(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.6G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |