Primary Site >> Stomach Cancer
Gene >> SMARCA5
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000283131 |
| Start | 143545973:143545973(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2446G>A |
| AA Mutation | p.Glu816Lys(p.E816K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000283131 |
| Start | 143550045:143550045(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3034A>C |
| AA Mutation | p.Asn1012His(p.N1012H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000283131 |
| Start | 143538846:143538846(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs778415632 |
| CDS Mutation | c.1678C>T |
| AA Mutation | p.Arg560Cys(p.R560C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000283131 |
| Start | 143543632:143543632(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2027G>A |
| AA Mutation | p.Gly676Asp(p.G676D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000283131 |
| Start | 143547474:143547474(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs778373183 |
| CDS Mutation | c.2743A>G |
| AA Mutation | p.Ile915Val(p.I915V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000283131 |
| Start | 143547425:143547425(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2694G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000283131 |
| Start | 143527885:143527885(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs78019012 |
| CDS Mutation | c.819C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000283131 |
| Start | 143545965:143545965(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.2442delA |
| AA Mutation | p.Glu815LysfsTer17(p.E815Kfs*17) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000283131 |
| Start | 143521556:143521557(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | novel |
| CDS Mutation | c.387dupA |
| AA Mutation | p.Asp130ArgfsTer2(p.D130Rfs*2) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |