Primary Site >> Stomach Cancer
Gene >> URI1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000392271 |
| Start | 30009249:30009249(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs769862941 |
| CDS Mutation | c.931G>A |
| AA Mutation | p.Asp311Asn(p.D311N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000392271 |
| Start | 30011157:30011157(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs778158912 |
| CDS Mutation | c.1099C>T |
| AA Mutation | p.Arg367Cys(p.R367C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000392271 |
| Start | 30012312:30012312(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1206A>T |
| AA Mutation | p.Glu402Asp(p.E402D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000392271 |
| Start | 30009013:30009013(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.695A>C |
| AA Mutation | p.Asp232Ala(p.D232A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000392271 |
| Start | 30015037:30015037(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1576T>C |
| AA Mutation | p.Phe526Leu(p.F526L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000392271 |
| Start | 30014984:30014984(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs763301059 |
| CDS Mutation | c.1523G>A |
| AA Mutation | p.Arg508Gln(p.R508Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000392271 |
| Start | 30011119:30011119(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1061C>T |
| AA Mutation | p.Thr354Ile(p.T354I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000392271 |
| Start | 30009261:30009261(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.943G>A |
| AA Mutation | p.Asp315Asn(p.D315N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000392271 |
| Start | 30009248:30009248(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs745994162 |
| CDS Mutation | c.930C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000392271 |
| Start | 29971219:29971219(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.144C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000392271 |
| Start | 30012414:30012414(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1308A>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000392271 |
| Start | 30011219:30011219(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs200788387 |
| CDS Mutation | c.1161G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |