Primary Site >> Stomach Cancer
Gene >> TLR7
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000380659 |
| Start | 12886965:12886965(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1457C>A |
| AA Mutation | p.Ser486Tyr(p.S486Y) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000380659 |
| Start | 12885599:12885599(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.91C>T |
| AA Mutation | p.Pro31Ser(p.P31S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000380659 |
| Start | 12888403:12888403(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2895A>C |
| AA Mutation | p.Glu965Asp(p.E965D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000380659 |
| Start | 12888260:12888260(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2752G>T |
| AA Mutation | p.Asp918Tyr(p.D918Y) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000380659 |
| Start | 12887954:12887954(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2446G>T |
| AA Mutation | p.Gly816Trp(p.G816W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000380659 |
| Start | 12886372:12886372(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs368187775 |
| CDS Mutation | c.864G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000380659 |
| Start | 12885943:12885943(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.435C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000380659 |
| Start | 12887299:12887299(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1791T>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000380659 |
| Start | 12887024:12887024(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | rs764545107 |
| CDS Mutation | c.1521delT |
| AA Mutation | p.Phe507LeufsTer16(p.F507Lfs*16) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000380659 |
| Start | 12887756:12887756(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs200283411 |
| CDS Mutation | c.2248C>T |
| AA Mutation | p.Arg750Ter(p.R750*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |