Primary Site >> Stomach Cancer
Gene >> NFKB2
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000369966 |
| Start | 102397342:102397342(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.436A>G |
| AA Mutation | p.Met146Val(p.M146V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000369966 |
| Start | 102401504:102401504(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs759429094 |
| CDS Mutation | c.2279C>T |
| AA Mutation | p.Pro760Leu(p.P760L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000369966 |
| Start | 102397602:102397602(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.578G>A |
| AA Mutation | p.Arg193His(p.R193H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000369966 |
| Start | 102401479:102401479(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2254A>T |
| AA Mutation | p.Asn752Tyr(p.N752Y) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000369966 |
| Start | 102400090:102400090(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1480C>A |
| AA Mutation | p.Leu494Ile(p.L494I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000369966 |
| Start | 102401031:102401031(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2053C>T |
| AA Mutation | p.Arg685Cys(p.R685C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000369966 |
| Start | 102400331:102400331(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1638G>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000369966 |
| Start | 102400152:102400152(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1542C>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000369966 |
| Start | 102398406:102398406(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | null |
| CDS Mutation | c.879delC |
| AA Mutation | p.Tyr294IlefsTer4(p.Y294Ifs*4) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000369966 |
| Start | 102401230:102401230(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | rs758282915 |
| CDS Mutation | c.2126delC |
| AA Mutation | p.Pro709LeufsTer34(p.P709Lfs*34) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | frameshift_variant;splice_region_variant |
| Transcription ID | ENST00000369966 |
| Start | 102401450:102401450(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.2225delT |
| AA Mutation | p.Val742GlyfsTer6(p.V742Gfs*6) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |