Primary Site >> Stomach Cancer
Gene >> TNFSF11
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000398795 |
| Start | 42600779:42600779(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs200862293 |
| CDS Mutation | c.415C>T |
| AA Mutation | p.His139Tyr(p.H139Y) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000398795 |
| Start | 42606892:42606892(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.928G>A |
| AA Mutation | p.Ala310Thr(p.A310T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000398795 |
| Start | 42606685:42606685(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.721T>C |
| AA Mutation | p.Tyr241His(p.Y241H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000398795 |
| Start | 42606792:42606792(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs199774248 |
| CDS Mutation | c.828C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000398795 |
| Start | 42600968:42600968(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs781456433 |
| CDS Mutation | c.519C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000398795 |
| Start | 42606501:42606501(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.537C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000398795 |
| Start | 42581251:42581251(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.345A>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000398795 |
| Start | 42606802:42606802(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.843delT |
| AA Mutation | p.Phe281LeufsTer36(p.F281Lfs*36) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |