Primary Site >> Stomach Cancer
Gene >> FAS
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000355740 |
| Start | 89014266:89014266(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.824T>C |
| AA Mutation | p.Val275Ala(p.V275A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000355740 |
| Start | 89014395:89014395(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.953T>A |
| AA Mutation | p.Ile318Asn(p.I318N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000355740 |
| Start | 89008951:89008951(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | null |
| CDS Mutation | c.403delT |
| AA Mutation | p.Cys135ValfsTer52(p.C135Vfs*52) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000355740 |
| Start | 89014337:89014337(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.900delA |
| AA Mutation | p.Ala301ProfsTer60(p.A301Pfs*60) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000355740 |
| Start | 89014285:89014285(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.843G>A |
| AA Mutation | p.Trp281Ter(p.W281*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000355740 |
| Start | 89008950:89008951(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | null |
| CDS Mutation | c.403dupT |
| AA Mutation | p.Cys135LeufsTer2(p.C135Lfs*2) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000355740 |
| Start | 89014134:89014135(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | rs606231366 |
| CDS Mutation | c.692_693insT |
| AA Mutation | p.Lys231AsnfsTer16(p.K231Nfs*16) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |