Primary Site >> Stomach Cancer
Gene >> TLR10
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000308973 |
| Start | 38775442:38775442(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.149C>T |
| AA Mutation | p.Thr50Ile(p.T50I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000308973 |
| Start | 38773348:38773348(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2243T>C |
| AA Mutation | p.Leu748Pro(p.L748P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000308973 |
| Start | 38774206:38774206(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1385C>A |
| AA Mutation | p.Thr462Asn(p.T462N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000308973 |
| Start | 38774968:38774968(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs147715812 |
| CDS Mutation | c.623G>A |
| AA Mutation | p.Arg208His(p.R208H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000308973 |
| Start | 38775029:38775029(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.562T>G |
| AA Mutation | p.Leu188Val(p.L188V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000308973 |
| Start | 38775539:38775539(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs762495806 |
| CDS Mutation | c.52G>A |
| AA Mutation | p.Glu18Lys(p.E18K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000308973 |
| Start | 38773685:38773685(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs776224049 |
| CDS Mutation | c.1906G>A |
| AA Mutation | p.Ala636Thr(p.A636T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000308973 |
| Start | 38773309:38773309(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2282G>T |
| AA Mutation | p.Arg761Met(p.R761M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000308973 |
| Start | 38774771:38774771(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.820T>C |
| AA Mutation | p.Phe274Leu(p.F274L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000308973 |
| Start | 38774547:38774547(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1044G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000308973 |
| Start | 38774340:38774340(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs374963343 |
| CDS Mutation | c.1251C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |