Primary Site >> Liver Cancer
Gene >> SMARCA2
| ID | 1 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000349721 |
| Start | 2070419:2070419(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1694A>C |
| AA Mutation | p.Lys565Thr(p.K565T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000349721 |
| Start | 2123922:2123922(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3966G>C |
| AA Mutation | p.Glu1322Asp(p.E1322D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000349721 |
| Start | 2182157:2182157(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.4376A>G |
| AA Mutation | p.His1459Arg(p.H1459R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000349721 |
| Start | 2101571:2101571(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3080A>C |
| AA Mutation | p.Glu1027Ala(p.E1027A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000349721 |
| Start | 2097385:2097385(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2992G>C |
| AA Mutation | p.Gly998Arg(p.G998R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000349721 |
| Start | 2123796:2123796(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs764977538 |
| CDS Mutation | c.3840G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | splice_acceptor_variant |
| Transcription ID | ENST00000349721 |
| Start | 2115820:2115820(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3457-2A>T |
| Mutation Classification | Splice_Site |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | splice_acceptor_variant |
| Transcription ID | ENST00000349721 |
| Start | 2097384:2097384(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2992-1G>T |
| Mutation Classification | Splice_Site |
| Feature Type | Transcript |