WormBase Tree Display for Variation: WBVar01973648
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| WBVar01973648 | Name | Public_name | WBVar01973648 | |||||
|---|---|---|---|---|---|---|---|---|
| Other_name | cewivar00699632 | |||||||
| F26F12.3c.1:c.*779dup | ||||||||
| F26F12.3b.3:c.*779dup | ||||||||
| F26F12.3b.1:c.*779dup | ||||||||
| F26F12.3b.2:c.*779dup | ||||||||
| F26F12.3a.1:c.*779dup | ||||||||
| HGVSg | CHROMOSOME_V:g.5839052_5839053insA | |||||||
| Sequence_details | SMap | S_parent | Sequence | F26F12 | ||||
| Flanking_sequences | AAACATATACACTAAAGCAAAATTGAATAC | AAAAAAAACACGATCTAGGCATATTAGATA | ||||||
| Mapping_target | F26F12 | |||||||
| Source_location | 225 | CHROMOSOME_V | 5839035 | 5839036 | From_analysis | Million_mutation_project_reanalysis | ||
| Type_of_mutation | Insertion | A | ||||||
| SeqStatus | Sequenced | |||||||
| Variation_type | Natural_variant | |||||||
| Origin | Species | Caenorhabditis elegans | ||||||
| Strain | WBStrain00004602 | From_analysis | Million_mutation_project_reanalysis | |||||
| WBStrain00006629 | From_analysis | Million_mutation_project_reanalysis | ||||||
| WBStrain00022850 | From_analysis | Million_mutation_project_reanalysis | ||||||
| WBStrain00023072 | From_analysis | Million_mutation_project_reanalysis | ||||||
| WBStrain00023139 | From_analysis | Million_mutation_project_reanalysis | ||||||
| WBStrain00027648 | From_analysis | Million_mutation_project_reanalysis | ||||||
| WBStrain00027660 | From_analysis | Million_mutation_project_reanalysis | ||||||
| WBStrain00027662 | From_analysis | Million_mutation_project_reanalysis | ||||||
| Laboratory | VC | |||||||
| Analysis | Million_mutation_project_reanalysis | |||||||
| Status | Live | |||||||
| Affects | Gene | WBGene00017834 | ||||||
| Transcript | F26F12.3b.1 | VEP_consequence | 3_prime_UTR_variant | |||||
| VEP_impact | MODIFIER | |||||||
| HGVSc | F26F12.3b.1:c.*779dup | |||||||
| cDNA_position | 3577-3578 | |||||||
| Exon_number | 7/7 | |||||||
| F26F12.3b.2 | VEP_consequence | 3_prime_UTR_variant | ||||||
| VEP_impact | MODIFIER | |||||||
| HGVSc | F26F12.3b.2:c.*779dup | |||||||
| cDNA_position | 3539-3540 | |||||||
| Exon_number | 7/7 | |||||||
| F26F12.3a.1 | VEP_consequence | 3_prime_UTR_variant | ||||||
| VEP_impact | MODIFIER | |||||||
| HGVSc | F26F12.3a.1:c.*779dup | |||||||
| cDNA_position | 3496-3497 | |||||||
| Exon_number | 7/7 | |||||||
| F26F12.3c.1 | VEP_consequence | 3_prime_UTR_variant | ||||||
| VEP_impact | MODIFIER | |||||||
| HGVSc | F26F12.3c.1:c.*779dup | |||||||
| cDNA_position | 4397-4398 | |||||||
| Exon_number | 7/7 | |||||||
| F26F12.3b.3 | VEP_consequence | 3_prime_UTR_variant | ||||||
| VEP_impact | MODIFIER | |||||||
| HGVSc | F26F12.3b.3:c.*779dup | |||||||
| cDNA_position | 3421-3422 | |||||||
| Exon_number | 6/6 | |||||||
| Method | WGS_Flibotte |
