Primary Site >> Esophagus Cancer
Gene >> PPL
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000345988 |
| Start | 4884232:4884232(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.4423C>A |
| AA Mutation | p.Leu1475Ile(p.L1475I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000345988 |
| Start | 4883514:4883514(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.5141A>T |
| AA Mutation | p.Lys1714Met(p.K1714M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000345988 |
| Start | 4899115:4899115(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.774C>G |
| AA Mutation | p.Phe258Leu(p.F258L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000345988 |
| Start | 4888127:4888127(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2489C>G |
| AA Mutation | p.Ser830Cys(p.S830C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000345988 |
| Start | 4885546:4885546(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs755310125 |
| CDS Mutation | c.3109C>T |
| AA Mutation | p.Arg1037Cys(p.R1037C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000345988 |
| Start | 4892145:4892145(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1719C>G |
| AA Mutation | p.Phe573Leu(p.F573L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000345988 |
| Start | 4888210:4888210(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2406G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |