Primary Site >> Stomach Cancer
Gene >> TERF1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000276603 |
| Start | 73022291:73022291(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs147608592 |
| CDS Mutation | c.613A>G |
| AA Mutation | p.Asn205Asp(p.N205D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000276603 |
| Start | 73022292:73022292(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.614A>C |
| AA Mutation | p.Asn205Thr(p.N205T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000276603 |
| Start | 73039162:73039162(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1086A>G |
| AA Mutation | p.Ile362Met(p.I362M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000276603 |
| Start | 73030356:73030356(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs533827129 |
| CDS Mutation | c.908C>T |
| AA Mutation | p.Ala303Val(p.A303V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000276603 |
| Start | 73046088:73046088(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1271G>T |
| AA Mutation | p.Trp424Leu(p.W424L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000276603 |
| Start | 73008941:73008941(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs769878289 |
| CDS Mutation | c.55A>G |
| AA Mutation | p.Arg19Gly(p.R19G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000276603 |
| Start | 73039183:73039183(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs199608164 |
| CDS Mutation | c.1107G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |