Primary Site >> Stomach Cancer
Gene >> SCARF2
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000622235 |
| Start | 20425940:20425940(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs746555186 |
| CDS Mutation | c.2036G>A |
| AA Mutation | p.Arg679His(p.R679H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000622235 |
| Start | 20431974:20431974(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.188C>T |
| AA Mutation | p.Thr63Met(p.T63M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000622235 |
| Start | 20425859:20425859(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2117C>T |
| AA Mutation | p.Ala706Val(p.A706V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000622235 |
| Start | 20429564:20429564(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1396G>A |
| AA Mutation | p.Ala466Thr(p.A466T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000622235 |
| Start | 20430869:20430869(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.894C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000622235 |
| Start | 20426032:20426032(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1944G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |