Primary Site >> Stomach Cancer
Gene >> ADAM9
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000487273 |
| Start | 38997116:38997116(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.53T>G |
| AA Mutation | p.Leu18Arg(p.L18R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000487273 |
| Start | 39054571:39054571(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs766583766 |
| CDS Mutation | c.1393C>T |
| AA Mutation | p.Arg465Trp(p.R465W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000487273 |
| Start | 39054517:39054517(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1339T>C |
| AA Mutation | p.Cys447Arg(p.C447R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000487273 |
| Start | 39016133:39016133(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs753966173 |
| CDS Mutation | c.349C>T |
| AA Mutation | p.Arg117Trp(p.R117W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000487273 |
| Start | 39055591:39055591(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1410T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000487273 |
| Start | 39077309:39077309(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs749882470 |
| CDS Mutation | c.1779G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000487273 |
| Start | 39017288:39017288(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.480C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000487273 |
| Start | 38997078:38997078(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs775495452 |
| CDS Mutation | c.15G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000487273 |
| Start | 38997090:38997090(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.30delG |
| AA Mutation | p.Thr11ProfsTer36(p.T11Pfs*36) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |