Primary Site >> Stomach Cancer
Gene >> BUB1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000302759 |
| Start | 110672719:110672719(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.364C>A |
| AA Mutation | p.Leu122Ile(p.L122I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000302759 |
| Start | 110661715:110661715(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1084G>T |
| AA Mutation | p.Val362Phe(p.V362F) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000302759 |
| Start | 110666324:110666324(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.896A>C |
| AA Mutation | p.Lys299Thr(p.K299T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000302759 |
| Start | 110650679:110650679(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2070G>T |
| AA Mutation | p.Glu690Asp(p.E690D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000302759 |
| Start | 110638000:110638000(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3222T>G |
| AA Mutation | p.Ile1074Met(p.I1074M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000302759 |
| Start | 110650629:110650629(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2120T>G |
| AA Mutation | p.Ile707Ser(p.I707S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000302759 |
| Start | 110661789:110661789(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs548365437 |
| CDS Mutation | c.1010C>T |
| AA Mutation | p.Ala337Val(p.A337V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000302759 |
| Start | 110674203:110674203(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs1801328 |
| CDS Mutation | c.108G>T |
| AA Mutation | p.Glu36Asp(p.E36D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000302759 |
| Start | 110650749:110650749(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2000C>T |
| AA Mutation | p.Ser667Leu(p.S667L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000302759 |
| Start | 110641680:110641680(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2587G>C |
| AA Mutation | p.Val863Leu(p.V863L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000302759 |
| Start | 110655861:110655861(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs375036331 |
| CDS Mutation | c.1754G>A |
| AA Mutation | p.Arg585His(p.R585H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000302759 |
| Start | 110657587:110657587(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1575T>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000302759 |
| Start | 110653492:110653492(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs77633848 |
| CDS Mutation | c.1908G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000302759 |
| Start | 110641429:110641429(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.2661delA |
| AA Mutation | p.Val888Ter(p.V888*) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |