Primary Site >> Stomach Cancer
Gene >> TMEM11
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000317635 |
| Start | 21198632:21198632(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs202195850 |
| CDS Mutation | c.271G>A |
| AA Mutation | p.Ala91Thr(p.A91T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000317635 |
| Start | 21198341:21198341(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs775552645 |
| CDS Mutation | c.562G>A |
| AA Mutation | p.Glu188Lys(p.E188K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000317635 |
| Start | 21198380:21198380(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.523G>A |
| AA Mutation | p.Ala175Thr(p.A175T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000317635 |
| Start | 21198637:21198637(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.266G>A |
| AA Mutation | p.Gly89Asp(p.G89D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000317635 |
| Start | 21198639:21198639(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs369634383 |
| CDS Mutation | c.264G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000317635 |
| Start | 21198471:21198471(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs749474774 |
| CDS Mutation | c.432G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |