Primary Site >> Esophagus Cancer
Gene >> PER2
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000254657 |
| Start | 238253619:238253619(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2404G>A |
| AA Mutation | p.Val802Ile(p.V802I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000254657 |
| Start | 238275850:238275850(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.341C>T |
| AA Mutation | p.Thr114Ile(p.T114I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | splice_donor_variant;intron_variant |
| Transcription ID | ENST00000254657 |
| Start | 238268031:238268054(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.967+2_967+25delTAACAGCCAAGCCCAGGGCGAGGG |
| Mutation Classification | Splice_Site |
| Feature Type | Transcript |