WormBase Tree Display for Variation: WBVar00266976
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| WBVar00266976 | Evidence | Paper_evidence | WBPaper00005369 | ||
|---|---|---|---|---|---|
| Name | Public_name | WBVar00266976 | |||
| Other_name | uCE1-800 | ||||
| C09D1.1f.1:c.796-979dup | |||||
| C09D1.1e.1:c.796-979dup | |||||
| C09D1.1o.1:c.796-979dup | |||||
| C09D1.1n.1:c.796-979dup | |||||
| C09D1.1a.1:c.796-979dup | |||||
| C09D1.1k.1:c.796-979dup | |||||
| C09D1.1b.1:c.796-979dup | |||||
| C09D1.1l.1:c.796-979dup | |||||
| C09D1.1m.1:c.796-979dup | |||||
| HGVSg | CHROMOSOME_I:g.4043821dup | ||||
| Sequence_details | SMap | S_parent | Sequence | C09D1 | |
| Flanking_sequences | ATGCTGCTCTTTCGCTTTTTTCTTCTGTAAAAATCTCCAAGAACCCAATATTTTCTCTTGTTTTAATCTGAAATGTCATATTAAAAATTTTCTTTTTTTT | CTTTTTCTCACTATCAATTTATTCAAATTTGATTAAGATCTCTCTCTACTAAAGTCTACTGAAGCTAACCTTAACGACGTTGTTTGGAAAAACTATGGTTC | |||
| Mapping_target | C09D1 | ||||
| Type_of_mutation | Insertion | T | |||
| SeqStatus | Sequenced | ||||
| Variation_type | SNP | ||||
| Predicted_SNP | |||||
| Natural_variant | |||||
| Origin | Species | Caenorhabditis elegans | |||
| Strain | WBStrain00004602 | From_analysis | SNP_Swan | ||
| Analysis | SNP_Swan | ||||
| Status | Live | ||||
| Affects | Gene | WBGene00006820 | |||
| Transcript | C09D1.1b.1 | VEP_consequence | intron_variant | ||
| VEP_impact | MODIFIER | ||||
| HGVSc | C09D1.1b.1:c.796-979dup | ||||
| Intron_number | 5/48 | ||||
| C09D1.1o.1 | VEP_consequence | intron_variant | |||
| VEP_impact | MODIFIER | ||||
| HGVSc | C09D1.1o.1:c.796-979dup | ||||
| Intron_number | 5/32 | ||||
| C09D1.1k.1 | VEP_consequence | intron_variant | |||
| VEP_impact | MODIFIER | ||||
| HGVSc | C09D1.1k.1:c.796-979dup | ||||
| Intron_number | 5/46 | ||||
| C09D1.1l.1 | VEP_consequence | intron_variant | |||
| VEP_impact | MODIFIER | ||||
| HGVSc | C09D1.1l.1:c.796-979dup | ||||
| Intron_number | 5/32 | ||||
| C09D1.1n.1 | VEP_consequence | intron_variant | |||
| VEP_impact | MODIFIER | ||||
| HGVSc | C09D1.1n.1:c.796-979dup | ||||
| Intron_number | 5/46 | ||||
| C09D1.1a.1 | VEP_consequence | intron_variant | |||
| VEP_impact | MODIFIER | ||||
| HGVSc | C09D1.1a.1:c.796-979dup | ||||
| Intron_number | 6/35 | ||||
| C09D1.1e.1 | VEP_consequence | intron_variant | |||
| VEP_impact | MODIFIER | ||||
| HGVSc | C09D1.1e.1:c.796-979dup | ||||
| Intron_number | 5/31 | ||||
| C09D1.1f.1 | VEP_consequence | intron_variant | |||
| VEP_impact | MODIFIER | ||||
| HGVSc | C09D1.1f.1:c.796-979dup | ||||
| Intron_number | 5/45 | ||||
| C09D1.1m.1 | VEP_consequence | intron_variant | |||
| VEP_impact | MODIFIER | ||||
| HGVSc | C09D1.1m.1:c.796-979dup | ||||
| Intron_number | 5/47 | ||||
| Reference | WBPaper00005369 | ||||
| Method | SNP_Swan |
