WormBase Tree Display for Variation: WBVar01551598
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| WBVar01551598 | Name | Public_name | WBVar01551598 | |||||
|---|---|---|---|---|---|---|---|---|
| Other_name | cewivar00128655 | |||||||
| T06H11.1f.1:c.413-1034C>T | ||||||||
| T06H11.1c.1:c.149-1034C>T | ||||||||
| T06H11.1g.1:c.137-1034C>T | ||||||||
| T06H11.1e.1:c.67+707C>T | ||||||||
| T06H11.1d.1:c.293-1034C>T | ||||||||
| T06H11.1b.1:c.263-1034C>T | ||||||||
| HGVSg | CHROMOSOME_X:g.10110365G>A | |||||||
| Sequence_details | SMap | S_parent | Sequence | T06H11 | ||||
| Flanking_sequences | TTTCCTTAAATATTTCAAATTTTTAAAATT | ATTCTGAACTATGTTTTTTTATTGTCTTGA | ||||||
| Mapping_target | T06H11 | |||||||
| Source_location | 225 | CHROMOSOME_X | 10110306 | 10110306 | From_analysis | Million_mutation_project_reanalysis | ||
| Type_of_mutation | Substitution | G | A | |||||
| SeqStatus | Sequenced | |||||||
| Variation_type | Natural_variant | |||||||
| Origin | Species | Caenorhabditis elegans | ||||||
| Strain | WBStrain00004599 | From_analysis | Million_mutation_project_reanalysis | |||||
| WBStrain00022850 | From_analysis | Million_mutation_project_reanalysis | ||||||
| WBStrain00023139 | From_analysis | Million_mutation_project_reanalysis | ||||||
| WBStrain00023192 | From_analysis | Million_mutation_project_reanalysis | ||||||
| WBStrain00024204 | From_analysis | Million_mutation_project_reanalysis | ||||||
| WBStrain00027647 | From_analysis | Million_mutation_project_reanalysis | ||||||
| WBStrain00027648 | From_analysis | Million_mutation_project_reanalysis | ||||||
| WBStrain00027660 | From_analysis | Million_mutation_project_reanalysis | ||||||
| Laboratory | VC | |||||||
| Analysis | Million_mutation_project_reanalysis | |||||||
| Status | Live | |||||||
| Affects | Gene | WBGene00006792 | ||||||
| Transcript | T06H11.1b.1 | VEP_consequence | intron_variant | |||||
| VEP_impact | MODIFIER | |||||||
| HGVSc | T06H11.1b.1:c.263-1034C>T | |||||||
| Intron_number | 3/12 | |||||||
| T06H11.1g.1 | VEP_consequence | intron_variant | ||||||
| VEP_impact | MODIFIER | |||||||
| HGVSc | T06H11.1g.1:c.137-1034C>T | |||||||
| Intron_number | 2/12 | |||||||
| T06H11.1f.1 | VEP_consequence | intron_variant | ||||||
| VEP_impact | MODIFIER | |||||||
| HGVSc | T06H11.1f.1:c.413-1034C>T | |||||||
| Intron_number | 4/14 | |||||||
| T06H11.1e.1 | VEP_consequence | intron_variant | ||||||
| VEP_impact | MODIFIER | |||||||
| HGVSc | T06H11.1e.1:c.67+707C>T | |||||||
| Intron_number | 2/13 | |||||||
| T06H11.1d.1 | VEP_consequence | intron_variant | ||||||
| VEP_impact | MODIFIER | |||||||
| HGVSc | T06H11.1d.1:c.293-1034C>T | |||||||
| Intron_number | 1/11 | |||||||
| T06H11.1c.1 | VEP_consequence | intron_variant | ||||||
| VEP_impact | MODIFIER | |||||||
| HGVSc | T06H11.1c.1:c.149-1034C>T | |||||||
| Intron_number | 2/13 | |||||||
| Method | WGS_Flibotte |
