Primary Site >> Stomach Cancer
Gene >> TSC1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000298552 |
| Start | 132897519:132897519(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2717A>C |
| AA Mutation | p.Gln906Pro(p.Q906P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000298552 |
| Start | 132910689:132910689(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1145G>A |
| AA Mutation | p.Gly382Asp(p.G382D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000298552 |
| Start | 132905974:132905974(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1604C>A |
| AA Mutation | p.Pro535His(p.P535H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000298552 |
| Start | 132928809:132928809(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs749030456 |
| CDS Mutation | c.64C>T |
| AA Mutation | p.Arg22Trp(p.R22W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000298552 |
| Start | 132921964:132921964(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs777484049 |
| CDS Mutation | c.518C>T |
| AA Mutation | p.Ala173Val(p.A173V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000298552 |
| Start | 132910655:132910655(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1179C>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000298552 |
| Start | 132896430:132896430(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs754282309 |
| CDS Mutation | c.3300C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000298552 |
| Start | 132896535:132896535(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs118203746 |
| CDS Mutation | c.3195G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |