Primary Site >> Stomach Cancer
Gene >> PAQR4
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000318782 |
| Start | 2971596:2971596(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs367647268 |
| CDS Mutation | c.470C>T |
| AA Mutation | p.Ser157Leu(p.S157L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000318782 |
| Start | 2971677:2971677(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs764816418 |
| CDS Mutation | c.551G>A |
| AA Mutation | p.Arg184His(p.R184H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000318782 |
| Start | 2971824:2971824(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.698T>G |
| AA Mutation | p.Phe233Cys(p.F233C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000318782 |
| Start | 2971802:2971802(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs202239569 |
| CDS Mutation | c.676G>A |
| AA Mutation | p.Glu226Lys(p.E226K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000318782 |
| Start | 2971607:2971607(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs566373345 |
| CDS Mutation | c.481G>A |
| AA Mutation | p.Gly161Ser(p.G161S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000318782 |
| Start | 2971666:2971666(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.540G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |