WormBase Tree Display for Variation: WBVar01963032
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| WBVar01963032 | Name | Public_name | WBVar01963032 | |||||
|---|---|---|---|---|---|---|---|---|
| Other_name | cewivar00688922 | |||||||
| T21C12.1c.1:c.*543-100_*543-99insCT | ||||||||
| T21C12.1h.1:c.554-100_554-99insCT | ||||||||
| T21C12.1o.1:c.602-100_602-99insCT | ||||||||
| T21C12.1f.1:c.1106-100_1106-99insCT | ||||||||
| T21C12.1i.1:c.233-100_233-99insCT | ||||||||
| T21C12.1d.1:c.*543-100_*543-99insCT | ||||||||
| T21C12.1e.1:c.*543-100_*543-99insCT | ||||||||
| HGVSg | CHROMOSOME_III:g.10532109_10532110insCT | |||||||
| Sequence_details | SMap | S_parent | Sequence | T21C12 | ||||
| Flanking_sequences | TGTAGTTTTAACAGAAACTAGCTTTTTTAG | CCGCCCATTTTTTGGCTAAAACCCATTTTT | ||||||
| Mapping_target | T21C12 | |||||||
| Source_location | 225 | CHROMOSOME_III | 10532011 | 10532012 | From_analysis | Million_mutation_project_reanalysis | ||
| Type_of_mutation | Insertion | CT | ||||||
| SeqStatus | Sequenced | |||||||
| Variation_type | Natural_variant | |||||||
| Origin | Species | Caenorhabditis elegans | ||||||
| Strain | WBStrain00004602 | From_analysis | Million_mutation_project_reanalysis | |||||
| WBStrain00022850 | From_analysis | Million_mutation_project_reanalysis | ||||||
| WBStrain00023018 | From_analysis | Million_mutation_project_reanalysis | ||||||
| WBStrain00023138 | From_analysis | Million_mutation_project_reanalysis | ||||||
| Laboratory | VC | |||||||
| Analysis | Million_mutation_project_reanalysis | |||||||
| Status | Live | |||||||
| Affects | Gene | WBGene00006784 | ||||||
| Transcript | T21C12.1h.1 | VEP_consequence | intron_variant | |||||
| VEP_impact | MODIFIER | |||||||
| HGVSc | T21C12.1h.1:c.554-100_554-99insCT | |||||||
| Intron_number | 4/6 | |||||||
| T21C12.1o.1 | VEP_consequence | intron_variant | ||||||
| VEP_impact | MODIFIER | |||||||
| HGVSc | T21C12.1o.1:c.602-100_602-99insCT | |||||||
| Intron_number | 4/5 | |||||||
| T21C12.1i.1 | VEP_consequence | intron_variant | ||||||
| VEP_impact | MODIFIER | |||||||
| HGVSc | T21C12.1i.1:c.233-100_233-99insCT | |||||||
| Intron_number | 1/2 | |||||||
| T21C12.1d.1 | VEP_consequence | intron_variant | ||||||
| VEP_impact | MODIFIER | |||||||
| HGVSc | T21C12.1d.1:c.*543-100_*543-99insCT | |||||||
| Intron_number | 16/17 | |||||||
| T21C12.1c.1 | VEP_consequence | intron_variant | ||||||
| VEP_impact | MODIFIER | |||||||
| HGVSc | T21C12.1c.1:c.*543-100_*543-99insCT | |||||||
| Intron_number | 17/18 | |||||||
| T21C12.1e.1 | VEP_consequence | intron_variant | ||||||
| VEP_impact | MODIFIER | |||||||
| HGVSc | T21C12.1e.1:c.*543-100_*543-99insCT | |||||||
| Intron_number | 18/19 | |||||||
| T21C12.1f.1 | VEP_consequence | intron_variant | ||||||
| VEP_impact | MODIFIER | |||||||
| HGVSc | T21C12.1f.1:c.1106-100_1106-99insCT | |||||||
| Intron_number | 9/11 | |||||||
| Method | WGS_Flibotte |
