Primary Site >> Stomach Cancer
Gene >> ERVW-1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000493463 |
| Start | 92468973:92468973(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1409A>C |
| AA Mutation | p.Asn470Thr(p.N470T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000493463 |
| Start | 92470206:92470206(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.176C>T |
| AA Mutation | p.Thr59Ile(p.T59I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000493463 |
| Start | 92470236:92470236(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.146C>T |
| AA Mutation | p.Ala49Val(p.A49V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000493463 |
| Start | 92469509:92469509(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.873A>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000493463 |
| Start | 92469572:92469572(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.810delT |
| AA Mutation | p.Phe270LeufsTer11(p.F270Lfs*11) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000493463 |
| Start | 92469235:92469235(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs372010298 |
| CDS Mutation | c.1147C>T |
| AA Mutation | p.Arg383Ter(p.R383*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |