Primary Site >> Stomach Cancer
Gene >> GP1BA
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000329125 |
| Start | 4932667:4932667(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.63G>T |
| AA Mutation | p.Glu21Asp(p.E21D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000329125 |
| Start | 4932644:4932644(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.40T>G |
| AA Mutation | p.Leu14Val(p.L14V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000329125 |
| Start | 4933268:4933268(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.664C>A |
| AA Mutation | p.Pro222Thr(p.P222T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000329125 |
| Start | 4933302:4933302(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs755192403 |
| CDS Mutation | c.698G>A |
| AA Mutation | p.Arg233His(p.R233H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000329125 |
| Start | 4932742:4932742(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs750305979 |
| CDS Mutation | c.138G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000329125 |
| Start | 4934078:4934078(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | rs759573909 |
| CDS Mutation | c.1480delA |
| AA Mutation | p.Thr494ProfsTer59(p.T494Pfs*59) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000329125 |
| Start | 4933223:4933223(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | null |
| CDS Mutation | c.624delT |
| AA Mutation | p.Phe208LeufsTer48(p.F208Lfs*48) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000329125 |
| Start | 4934077:4934078(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | rs767665147 |
| CDS Mutation | c.1480dupA |
| AA Mutation | p.Thr494AsnfsTer4(p.T494Nfs*4) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |