Primary Site >> Stomach Cancer
Gene >> TCN1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000257264 |
| Start | 59853244:59853244(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1199C>G |
| AA Mutation | p.Thr400Ser(p.T400S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000257264 |
| Start | 59854818:59854818(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs748680318 |
| CDS Mutation | c.955G>A |
| AA Mutation | p.Ala319Thr(p.A319T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000257264 |
| Start | 59854662:59854662(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1111A>G |
| AA Mutation | p.Thr371Ala(p.T371A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000257264 |
| Start | 59862715:59862715(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.267T>A |
| AA Mutation | p.Asp89Glu(p.D89E) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000257264 |
| Start | 59854695:59854695(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1078A>G |
| AA Mutation | p.Ser360Gly(p.S360G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000257264 |
| Start | 59859244:59859244(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs754351048 |
| CDS Mutation | c.580G>A |
| AA Mutation | p.Ala194Thr(p.A194T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000257264 |
| Start | 59854767:59854767(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs201160706 |
| CDS Mutation | c.1006G>A |
| AA Mutation | p.Val336Ile(p.V336I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000257264 |
| Start | 59861633:59861633(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs139772818 |
| CDS Mutation | c.450C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |