Primary Site >> Pancreatic Cancer
Gene >> GRIA1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000285900 |
| Start | 153655854:153655854(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.681C>G |
| AA Mutation | p.His227Gln(p.H227Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000285900 |
| Start | 153494057:153494057(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.212C>T |
| AA Mutation | p.Thr71Ile(p.T71I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000285900 |
| Start | 153674638:153674638(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs771987779 |
| CDS Mutation | c.838C>T |
| AA Mutation | p.Arg280Trp(p.R280W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000285900 |
| Start | 153647037:153647037(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs370782311 |
| CDS Mutation | c.330G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000285900 |
| Start | 153677005:153677005(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs749706041 |
| CDS Mutation | c.873G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000285900 |
| Start | 153794717:153794717(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs768117586 |
| CDS Mutation | c.2367C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |