Primary Site >> Stomach Cancer
Gene >> GFI1B
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000339463 |
| Start | 132990901:132990901(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs762113108 |
| CDS Mutation | c.844G>A |
| AA Mutation | p.Gly282Arg(p.G282R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000339463 |
| Start | 132989782:132989782(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.689A>G |
| AA Mutation | p.Lys230Arg(p.K230R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000339463 |
| Start | 132989789:132989789(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs755412589 |
| CDS Mutation | c.696G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000339463 |
| Start | 132989852:132989852(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs755994673 |
| CDS Mutation | c.759C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000339463 |
| Start | 132988246:132988246(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs749039556 |
| CDS Mutation | c.288C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000339463 |
| Start | 132987412:132987412(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs768614274 |
| CDS Mutation | c.231G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000339463 |
| Start | 132989078:132989078(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.528C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000339463 |
| Start | 132987373:132987373(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs778912632 |
| CDS Mutation | c.192G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |