Primary Site >> Stomach Cancer
Gene >> PNPT1
| ID | 1 |
| Mutation Consequence | missense_variant;NMD_transcript_variant |
| Transcription ID | ENST00000415374 |
| Start | 55672920:55672920(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs143022417 |
| CDS Mutation | c.839C>T |
| AA Mutation | p.Ser280Leu(p.S280L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant;NMD_transcript_variant |
| Transcription ID | ENST00000415374 |
| Start | 55643395:55643395(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs758915545 |
| CDS Mutation | c.1937C>T |
| AA Mutation | p.Thr646Met(p.T646M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | synonymous_variant;NMD_transcript_variant |
| Transcription ID | ENST00000415374 |
| Start | 55645415:55645415(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs750328203 |
| CDS Mutation | c.1756T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | synonymous_variant;NMD_transcript_variant |
| Transcription ID | ENST00000415374 |
| Start | 55693677:55693677(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.147G>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | synonymous_variant;NMD_transcript_variant |
| Transcription ID | ENST00000415374 |
| Start | 55680719:55680719(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.558A>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant;NMD_transcript_variant |
| Transcription ID | ENST00000415374 |
| Start | 55643409:55643409(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs779794474 |
| CDS Mutation | c.1923G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |