WormBase Tree Display for Variation: WBVar02058448
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| WBVar02058448 | Name | Public_name | WBVar02058448 | |||||
|---|---|---|---|---|---|---|---|---|
| Other_name | cewivar00787682 | |||||||
| F56H11.1e.1:c.584-25_584-24insTTCCT | ||||||||
| F56H11.1c.1:c.584-25_584-24insTTCCT | ||||||||
| F56H11.1g.1:c.584-25_584-24insTTCCT | ||||||||
| F56H11.1a.1:c.583+257_583+258insTTCCT | ||||||||
| F56H11.1h.1:c.584-25_584-24insTTCCT | ||||||||
| F56H11.1d.1:c.583+257_583+258insTTCCT | ||||||||
| F56H11.1f.1:c.583+257_583+258insTTCCT | ||||||||
| F56H11.1b.1:c.583+257_583+258insTTCCT | ||||||||
| HGVSg | CHROMOSOME_IV:g.9542010_9542011insTTCCT | |||||||
| Sequence_details | SMap | S_parent | Sequence | F56H11 | ||||
| Flanking_sequences | CATCCATTCCCGGTCCTCTAGCTTACCCAC | ATACCTTTTGTGCTTCTCTTTCAGATCGTA | ||||||
| Mapping_target | F56H11 | |||||||
| Source_location | 225 | CHROMOSOME_IV | 9541993 | 9541994 | From_analysis | Million_mutation_project_reanalysis | ||
| Type_of_mutation | Insertion | TTCCT | ||||||
| SeqStatus | Sequenced | |||||||
| Variation_type | Natural_variant | |||||||
| Origin | Species | Caenorhabditis elegans | ||||||
| Strain | WBStrain00023072 | From_analysis | Million_mutation_project_reanalysis | |||||
| Laboratory | VC | |||||||
| Analysis | Million_mutation_project_reanalysis | |||||||
| Status | Live | |||||||
| Affects | Gene | WBGene00001403 | ||||||
| Transcript | F56H11.1e.1 | VEP_consequence | intron_variant | |||||
| VEP_impact | MODIFIER | |||||||
| HGVSc | F56H11.1e.1:c.584-25_584-24insTTCCT | |||||||
| Intron_number | 4/11 | |||||||
| F56H11.1d.1 | VEP_consequence | intron_variant | ||||||
| VEP_impact | MODIFIER | |||||||
| HGVSc | F56H11.1d.1:c.583+257_583+258insTTCCT | |||||||
| Intron_number | 4/11 | |||||||
| F56H11.1a.1 | VEP_consequence | intron_variant | ||||||
| VEP_impact | MODIFIER | |||||||
| HGVSc | F56H11.1a.1:c.583+257_583+258insTTCCT | |||||||
| Intron_number | 5/15 | |||||||
| F56H11.1g.1 | VEP_consequence | intron_variant | ||||||
| VEP_impact | MODIFIER | |||||||
| HGVSc | F56H11.1g.1:c.584-25_584-24insTTCCT | |||||||
| Intron_number | 5/15 | |||||||
| F56H11.1h.1 | VEP_consequence | intron_variant | ||||||
| VEP_impact | MODIFIER | |||||||
| HGVSc | F56H11.1h.1:c.584-25_584-24insTTCCT | |||||||
| Intron_number | 4/11 | |||||||
| F56H11.1c.1 | VEP_consequence | intron_variant | ||||||
| VEP_impact | MODIFIER | |||||||
| HGVSc | F56H11.1c.1:c.584-25_584-24insTTCCT | |||||||
| Intron_number | 5/15 | |||||||
| F56H11.1f.1 | VEP_consequence | intron_variant | ||||||
| VEP_impact | MODIFIER | |||||||
| HGVSc | F56H11.1f.1:c.583+257_583+258insTTCCT | |||||||
| Intron_number | 4/11 | |||||||
| F56H11.1b.1 | VEP_consequence | intron_variant | ||||||
| VEP_impact | MODIFIER | |||||||
| HGVSc | F56H11.1b.1:c.583+257_583+258insTTCCT | |||||||
| Intron_number | 5/15 | |||||||
| Method | WGS_Flibotte |
