Primary Site >> Stomach Cancer
Gene >> SYT1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000261205 |
| Start | 79353574:79353574(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.883C>A |
| AA Mutation | p.Leu295Met(p.L295M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000261205 |
| Start | 79292018:79292018(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.362A>G |
| AA Mutation | p.Asp121Gly(p.D121G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000261205 |
| Start | 79296105:79296105(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.511G>A |
| AA Mutation | p.Ala171Thr(p.A171T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000261205 |
| Start | 79217656:79217656(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.137A>C |
| AA Mutation | p.Lys46Thr(p.K46T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000261205 |
| Start | 79285840:79285840(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.220A>C |
| AA Mutation | p.Thr74Pro(p.T74P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000261205 |
| Start | 79299394:79299394(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.653C>T |
| AA Mutation | p.Ser218Leu(p.S218L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000261205 |
| Start | 79299434:79299434(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.693T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000261205 |
| Start | 79217576:79217576(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs754566512 |
| CDS Mutation | c.57G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000261205 |
| Start | 79299497:79299497(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.759delT |
| AA Mutation | p.Phe253LeufsTer4(p.F253Lfs*4) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000261205 |
| Start | 79444164:79444165(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | novel |
| CDS Mutation | c.1022dupA |
| AA Mutation | p.Asn341LysfsTer2(p.N341Kfs*2) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |