Primary Site >> Esophagus Cancer
Gene >> PIK3CA
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000263967 |
| Start | 179218303:179218303(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs104886003 |
| CDS Mutation | c.1633G>A |
| AA Mutation | p.Glu545Lys(p.E545K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000263967 |
| Start | 179234297:179234297(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs121913279 |
| CDS Mutation | c.3140A>T |
| AA Mutation | p.His1047Leu(p.H1047L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000263967 |
| Start | 179234297:179234297(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs121913279 |
| CDS Mutation | c.3140A>G |
| AA Mutation | p.His1047Arg(p.H1047R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000263967 |
| Start | 179234286:179234286(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs121913283 |
| CDS Mutation | c.3129G>A |
| AA Mutation | p.Met1043Ile(p.M1043I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000263967 |
| Start | 179218308:179218308(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1638G>C |
| AA Mutation | p.Gln546His(p.Q546H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000263967 |
| Start | 179221146:179221146(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2176G>A |
| AA Mutation | p.Glu726Lys(p.E726K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000263967 |
| Start | 179230063:179230063(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2726T>G |
| AA Mutation | p.Phe909Cys(p.F909C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000263967 |
| Start | 179199690:179199690(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs587777790 |
| CDS Mutation | c.353G>A |
| AA Mutation | p.Gly118Asp(p.G118D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |