Primary Site >> Stomach Cancer
Gene >> TLR5
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000366881 |
| Start | 223112184:223112184(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.848C>G |
| AA Mutation | p.Ala283Gly(p.A283G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000366881 |
| Start | 223110892:223110892(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2140C>G |
| AA Mutation | p.His714Asp(p.H714D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000366881 |
| Start | 223111042:223111042(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs768801743 |
| CDS Mutation | c.1990C>T |
| AA Mutation | p.Arg664Trp(p.R664W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000366881 |
| Start | 223112442:223112442(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs146146738 |
| CDS Mutation | c.590C>T |
| AA Mutation | p.Thr197Met(p.T197M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000366881 |
| Start | 223112422:223112422(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.610G>T |
| AA Mutation | p.Ala204Ser(p.A204S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000366881 |
| Start | 223112587:223112587(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs201906412 |
| CDS Mutation | c.445C>T |
| AA Mutation | p.Arg149Cys(p.R149C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000366881 |
| Start | 223112931:223112931(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs187499609 |
| CDS Mutation | c.101G>A |
| AA Mutation | p.Arg34His(p.R34H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000366881 |
| Start | 223110666:223110666(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2366T>C |
| AA Mutation | p.Met789Thr(p.M789T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000366881 |
| Start | 223112586:223112586(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs372708351 |
| CDS Mutation | c.446G>A |
| AA Mutation | p.Arg149His(p.R149H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000366881 |
| Start | 223112202:223112202(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs752276249 |
| CDS Mutation | c.830C>A |
| AA Mutation | p.Pro277His(p.P277H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000366881 |
| Start | 223112831:223112831(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.201C>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000366881 |
| Start | 223112018:223112018(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1014C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000366881 |
| Start | 223111757:223111757(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs550493136 |
| CDS Mutation | c.1275G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000366881 |
| Start | 223110609:223110609(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.2423delG |
| AA Mutation | p.Gly808AlafsTer9(p.G808Afs*9) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000366881 |
| Start | 223111253:223111253(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1779G>A |
| AA Mutation | p.Trp593Ter(p.W593*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |