Primary Site >> Stomach Cancer
Gene >> NFKB1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000394820 |
| Start | 102580600:102580600(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.793G>T |
| AA Mutation | p.Gly265Trp(p.G265W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000394820 |
| Start | 102606595:102606595(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1849T>G |
| AA Mutation | p.Ser617Ala(p.S617A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000394820 |
| Start | 102596185:102596185(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1345A>C |
| AA Mutation | p.Ser449Arg(p.S449R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000394820 |
| Start | 102606604:102606604(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1858C>T |
| AA Mutation | p.His620Tyr(p.H620Y) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000394820 |
| Start | 102593495:102593495(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1134T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000394820 |
| Start | 102601000:102601000(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs190121351 |
| CDS Mutation | c.1740T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000394820 |
| Start | 102596182:102596182(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.1345delA |
| AA Mutation | p.Ser449ValfsTer7(p.S449Vfs*7) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000394820 |
| Start | 102616442:102616442(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2755C>T |
| AA Mutation | p.Arg919Ter(p.R919*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | protein_altering_variant |
| Transcription ID | ENST00000394820 |
| Start | 102606667:102606668(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | novel |
| CDS Mutation | c.1921_1922insGAGATT |
| AA Mutation | p.Ala641delinsGlyAspSer(p.A641delinsGDS) |
| Mutation Classification | In_Frame_Ins |
| Feature Type | Transcript |