Primary Site >> Stomach Cancer
Gene >> ITGB3
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000559488 |
| Start | 47302777:47302777(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs534325095 |
| CDS Mutation | c.2071G>A |
| AA Mutation | p.Val691Ile(p.V691I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000559488 |
| Start | 47292421:47292421(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs150138754 |
| CDS Mutation | c.1543C>T |
| AA Mutation | p.Arg515Trp(p.R515W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000559488 |
| Start | 47292485:47292485(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1607G>A |
| AA Mutation | p.Ser536Asn(p.S536N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000559488 |
| Start | 47284695:47284695(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.614A>C |
| AA Mutation | p.Asp205Ala(p.D205A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000559488 |
| Start | 47300523:47300523(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs112717328 |
| CDS Mutation | c.1959C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000559488 |
| Start | 47299381:47299381(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs763874595 |
| CDS Mutation | c.1764G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000559488 |
| Start | 47299429:47299429(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs769950254 |
| CDS Mutation | c.1812C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000559488 |
| Start | 47307589:47307589(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2253A>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000559488 |
| Start | 47284450:47284450(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs141225656 |
| CDS Mutation | c.369G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000559488 |
| Start | 47289723:47289723(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.986delA |
| AA Mutation | p.Asn329ThrfsTer4(p.N329Tfs*4) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000559488 |
| Start | 47292552:47292552(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | rs766268682 |
| CDS Mutation | c.1678delG |
| AA Mutation | p.Glu560ArgfsTer109(p.E560Rfs*109) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | splice_donor_variant;coding_sequence_variant;intron_variant |
| Transcription ID | ENST00000559488 |
| Start | 47289752:47289803(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.1013_1035+29delAAAATGTAGTCAATCTCTATCAGGTGACTGTGCCTTCGGGCTTCCTGGAGTG |
| Mutation Classification | Splice_Site |
| Feature Type | Transcript |