Primary Site >> Stomach Cancer
Gene >> B2M
| ID | 1 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000558401 |
| Start | 44715496:44715496(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.141G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000558401 |
| Start | 44715549:44715553(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.197_201delTTGAA |
| AA Mutation | p.Ile66LysfsTer22(p.I66Kfs*22) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000558401 |
| Start | 44711588:44711591(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | null |
| CDS Mutation | c.45_48delTTCT |
| AA Mutation | p.Ser16AlafsTer27(p.S16Afs*27) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000558401 |
| Start | 44715555:44715555(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | null |
| CDS Mutation | c.204delA |
| AA Mutation | p.Val69TrpfsTer34(p.V69Wfs*34) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000558401 |
| Start | 44715673:44715674(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.319_320delTT |
| AA Mutation | p.Leu107ValfsTer7(p.L107Vfs*7) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000558401 |
| Start | 44711583:44711586(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.41_44delCTCT |
| AA Mutation | p.Ser14PhefsTer29(p.S14Ffs*29) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000558401 |
| Start | 44715636:44715636(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | null |
| CDS Mutation | c.285delA |
| AA Mutation | p.Asp96MetfsTer7(p.D96Mfs*7) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000558401 |
| Start | 44715542:44715542(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.187G>T |
| AA Mutation | p.Gly63Ter(p.G63*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000558401 |
| Start | 44715698:44715699(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | novel |
| CDS Mutation | c.346+1dupG |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000558401 |
| Start | 44715626:44715627(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | null |
| CDS Mutation | c.276dupC |
| AA Mutation | p.Thr93HisfsTer2(p.T93Hfs*2) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000558401 |
| Start | 44715635:44715636(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | novel |
| CDS Mutation | c.285dupA |
| AA Mutation | p.Asp96ArgfsTer2(p.D96Rfs*2) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | splice_donor_variant |
| Transcription ID | ENST00000558401 |
| Start | 44711614:44711614(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.67+1G>A |
| Mutation Classification | Splice_Site |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | splice_acceptor_variant |
| Transcription ID | ENST00000558401 |
| Start | 44715421:44715421(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs111482205 |
| CDS Mutation | c.68-2A>G |
| Mutation Classification | Splice_Site |
| Feature Type | Transcript |