Primary Site >> Stomach Cancer
Gene >> PIK3R2
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000222254 |
| Start | 18160942:18160942(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs768743781 |
| CDS Mutation | c.439C>T |
| AA Mutation | p.Arg147Cys(p.R147C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000222254 |
| Start | 18167281:18167281(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1711C>T |
| AA Mutation | p.Arg571Cys(p.R571C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000222254 |
| Start | 18166266:18166266(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs143821279 |
| CDS Mutation | c.1523G>A |
| AA Mutation | p.Arg508His(p.R508H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000222254 |
| Start | 18166277:18166277(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1534G>A |
| AA Mutation | p.Glu512Lys(p.E512K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000222254 |
| Start | 18166265:18166265(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs376215289 |
| CDS Mutation | c.1522C>T |
| AA Mutation | p.Arg508Cys(p.R508C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000222254 |
| Start | 18168806:18168806(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs757901079 |
| CDS Mutation | c.1889C>T |
| AA Mutation | p.Thr630Met(p.T630M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000222254 |
| Start | 18162474:18162474(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1077C>G |
| AA Mutation | p.Ser359Arg(p.S359R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000222254 |
| Start | 18162430:18162430(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1033C>T |
| AA Mutation | p.Arg345Trp(p.R345W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000222254 |
| Start | 18163017:18163017(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1160A>G |
| AA Mutation | p.Tyr387Cys(p.Y387C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000222254 |
| Start | 18163320:18163320(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1348C>T |
| AA Mutation | p.His450Tyr(p.H450Y) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000222254 |
| Start | 18168881:18168881(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs762499879 |
| CDS Mutation | c.1964A>G |
| AA Mutation | p.Tyr655Cys(p.Y655C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000222254 |
| Start | 18169246:18169246(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs751700743 |
| CDS Mutation | c.2139G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |