Primary Site >> Stomach Cancer
Gene >> PRNP
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000379440 |
| Start | 4699530:4699530(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.310A>G |
| AA Mutation | p.Lys104Glu(p.K104E) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000379440 |
| Start | 4699950:4699950(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.730A>T |
| AA Mutation | p.Ile244Phe(p.I244F) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000379440 |
| Start | 4699606:4699606(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs779528653 |
| CDS Mutation | c.386T>C |
| AA Mutation | p.Met129Thr(p.M129T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000379440 |
| Start | 4699842:4699842(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs55826236 |
| CDS Mutation | c.622C>T |
| AA Mutation | p.Arg208Cys(p.R208C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000379440 |
| Start | 4699845:4699845(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs758820257 |
| CDS Mutation | c.625G>A |
| AA Mutation | p.Val209Met(p.V209M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000379440 |
| Start | 4699671:4699671(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs755417301 |
| CDS Mutation | c.451C>T |
| AA Mutation | p.Arg151Cys(p.R151C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000379440 |
| Start | 4699874:4699874(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs375057882 |
| CDS Mutation | c.654C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000379440 |
| Start | 4699757:4699757(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs755183662 |
| CDS Mutation | c.537C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000379440 |
| Start | 4699469:4699469(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.249G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000379440 |
| Start | 4699337:4699337(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs771206868 |
| CDS Mutation | c.117G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000379440 |
| Start | 4699784:4699784(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs201447742 |
| CDS Mutation | c.564G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |