Primary Site >> Esophagus Cancer
Gene >> PLCE1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000260766 |
| Start | 94298620:94298620(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs755528503 |
| CDS Mutation | c.5409G>A |
| AA Mutation | p.Met1803Ile(p.M1803I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000260766 |
| Start | 94273625:94273625(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs764087748 |
| CDS Mutation | c.4570A>G |
| AA Mutation | p.Met1524Val(p.M1524V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000260766 |
| Start | 94234071:94234071(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1973A>T |
| AA Mutation | p.Lys658Ile(p.K658I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000260766 |
| Start | 94132282:94132282(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1315G>T |
| AA Mutation | p.Gly439Cys(p.G439C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000260766 |
| Start | 94298391:94298391(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.5180G>A |
| AA Mutation | p.Gly1727Asp(p.G1727D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000260766 |
| Start | 94324361:94324361(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.6514G>A |
| AA Mutation | p.Ala2172Thr(p.A2172T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000260766 |
| Start | 94262666:94262666(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3987C>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000260766 |
| Start | 94270567:94270567(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs773520472 |
| CDS Mutation | c.4471T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000260766 |
| Start | 94234171:94234171(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2073G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |