Primary Site >> Stomach Cancer
Gene >> UHRF2
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000276893 |
| Start | 6498070:6498070(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1820G>A |
| AA Mutation | p.Arg607His(p.R607H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000276893 |
| Start | 6506085:6506085(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2315G>A |
| AA Mutation | p.Arg772Gln(p.R772Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000276893 |
| Start | 6498129:6498129(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1879C>T |
| AA Mutation | p.Arg627Trp(p.R627W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000276893 |
| Start | 6460623:6460623(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.695G>A |
| AA Mutation | p.Arg232Gln(p.R232Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000276893 |
| Start | 6434147:6434147(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs199593988 |
| CDS Mutation | c.618C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000276893 |
| Start | 6475403:6475403(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.876A>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000276893 |
| Start | 6486850:6486850(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs769255051 |
| CDS Mutation | c.1422T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000276893 |
| Start | 6504628:6504628(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs760957476 |
| CDS Mutation | c.2199C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |