Primary Site >> Stomach Cancer
Gene >> UVRAG
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000356136 |
| Start | 76141141:76141141(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1828A>G |
| AA Mutation | p.Ser610Gly(p.S610G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000356136 |
| Start | 75879924:75879924(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.316C>G |
| AA Mutation | p.Leu106Val(p.L106V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000356136 |
| Start | 76141312:76141312(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs138436357 |
| CDS Mutation | c.1999G>A |
| AA Mutation | p.Glu667Lys(p.E667K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000356136 |
| Start | 75983465:75983465(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs376568898 |
| CDS Mutation | c.778C>T |
| AA Mutation | p.Arg260Trp(p.R260W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000356136 |
| Start | 76065779:76065779(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1296T>G |
| AA Mutation | p.Asn432Lys(p.N432K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000356136 |
| Start | 75851893:75851893(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.128G>A |
| AA Mutation | p.Arg43Gln(p.R43Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000356136 |
| Start | 76141134:76141134(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1821G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000356136 |
| Start | 76115944:76115944(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1326A>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | frameshift_variant;splice_region_variant |
| Transcription ID | ENST00000356136 |
| Start | 75983387:75983387(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | rs770844823 |
| CDS Mutation | c.709delA |
| AA Mutation | p.Ser237ValfsTer6(p.S237Vfs*6) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |