Primary Site >> Stomach Cancer
Gene >> CBX4
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000269397 |
| Start | 79834227:79834227(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1415C>T |
| AA Mutation | p.Pro472Leu(p.P472L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000269397 |
| Start | 79834131:79834131(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs376832453 |
| CDS Mutation | c.1511C>T |
| AA Mutation | p.Ala504Val(p.A504V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000269397 |
| Start | 79834936:79834936(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs768157778 |
| CDS Mutation | c.706G>A |
| AA Mutation | p.Ala236Thr(p.A236T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000269397 |
| Start | 79835204:79835204(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.438G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000269397 |
| Start | 79834130:79834130(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1512G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000269397 |
| Start | 79835309:79835309(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs142055924 |
| CDS Mutation | c.333G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |