Primary Site >> Stomach Cancer
Gene >> TAP1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000354258 |
| Start | 32845665:32845665(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2341C>T |
| AA Mutation | p.Arg781Trp(p.R781W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000354258 |
| Start | 32852475:32852475(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.806G>A |
| AA Mutation | p.Gly269Asp(p.G269D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000354258 |
| Start | 32850452:32850452(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1296G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000354258 |
| Start | 32853136:32853136(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.681C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000354258 |
| Start | 32853577:32853577(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.240C>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000354258 |
| Start | 32853271:32853271(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.546delC |
| AA Mutation | p.Ser184ProfsTer54(p.S184Pfs*54) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000354258 |
| Start | 32851119:32851119(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.1055delC |
| AA Mutation | p.Thr352SerfsTer4(p.T352Sfs*4) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000354258 |
| Start | 32847980:32847980(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.1859delG |
| AA Mutation | p.Gly620AspfsTer44(p.G620Dfs*44) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000354258 |
| Start | 32853092:32853093(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | novel |
| CDS Mutation | c.724dupT |
| AA Mutation | p.Ser242PhefsTer32(p.S242Ffs*32) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000354258 |
| Start | 32852125:32852126(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | rs768903065 |
| CDS Mutation | c.1007dupT |
| AA Mutation | p.Gln337ProfsTer7(p.Q337Pfs*7) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |