Primary Site >> Stomach Cancer
Gene >> DCAF15
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000254337 |
| Start | 13956005:13956005(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs755588798 |
| CDS Mutation | c.460G>A |
| AA Mutation | p.Val154Ile(p.V154I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000254337 |
| Start | 13959617:13959617(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1255G>A |
| AA Mutation | p.Val419Met(p.V419M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000254337 |
| Start | 13959125:13959125(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.865C>T |
| AA Mutation | p.Pro289Ser(p.P289S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000254337 |
| Start | 13959202:13959202(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.942G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000254337 |
| Start | 13956207:13956207(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs372032476 |
| CDS Mutation | c.558C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000254337 |
| Start | 13959405:13959408(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.1145_1148delCCGA |
| AA Mutation | p.Ser382CysfsTer37(p.S382Cfs*37) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |