Primary Site >> Stomach Cancer
Gene >> YY1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000262238 |
| Start | 100239666:100239666(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs748178185 |
| CDS Mutation | c.422G>A |
| AA Mutation | p.Gly141Asp(p.G141D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000262238 |
| Start | 100277490:100277490(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1135G>A |
| AA Mutation | p.Gly379Arg(p.G379R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000262238 |
| Start | 100276554:100276554(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.968G>C |
| AA Mutation | p.Arg323Thr(p.R323T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000262238 |
| Start | 100262430:100262430(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.806A>G |
| AA Mutation | p.Asp269Gly(p.D269G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000262238 |
| Start | 100262407:100262407(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.783T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000262238 |
| Start | 100262307:100262307(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | rs759536629 |
| CDS Mutation | c.690delA |
| AA Mutation | p.Asp231IlefsTer25(p.D231Ifs*25) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |