Primary Site >> Stomach Cancer
Gene >> PIK3R5
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000447110 |
| Start | 8888285:8888285(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs540270770 |
| CDS Mutation | c.1502G>A |
| AA Mutation | p.Arg501His(p.R501H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000447110 |
| Start | 8887612:8887612(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs267605109 |
| CDS Mutation | c.1688G>A |
| AA Mutation | p.Arg563Gln(p.R563Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000447110 |
| Start | 8888282:8888282(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs775810359 |
| CDS Mutation | c.1505G>A |
| AA Mutation | p.Arg502His(p.R502H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000447110 |
| Start | 8889982:8889982(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.802G>A |
| AA Mutation | p.Gly268Arg(p.G268R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000447110 |
| Start | 8911469:8911469(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs777086538 |
| CDS Mutation | c.26C>T |
| AA Mutation | p.Thr9Met(p.T9M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000447110 |
| Start | 8890845:8890845(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.550A>G |
| AA Mutation | p.Thr184Ala(p.T184A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000447110 |
| Start | 8890008:8890008(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs369083136 |
| CDS Mutation | c.776C>T |
| AA Mutation | p.Ala259Val(p.A259V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000447110 |
| Start | 8886234:8886234(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2123C>T |
| AA Mutation | p.Ala708Val(p.A708V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000447110 |
| Start | 8888294:8888294(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs765654812 |
| CDS Mutation | c.1493G>A |
| AA Mutation | p.Arg498His(p.R498H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000447110 |
| Start | 8890765:8890765(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs773571409 |
| CDS Mutation | c.630C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000447110 |
| Start | 8888398:8888398(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs767011724 |
| CDS Mutation | c.1389G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |