WormBase Tree Display for Variation: WBVar01607469
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| WBVar01607469 | Name | Public_name | WBVar01607469 | |||||
|---|---|---|---|---|---|---|---|---|
| Other_name | cewivar00286545 | |||||||
| F18F11.3h.1:c.4026+11G>T | ||||||||
| F18F11.3e.1:c.3933+11G>T | ||||||||
| F18F11.3b.1:c.3738+11G>T | ||||||||
| F18F11.3f.1:c.3738+11G>T | ||||||||
| F18F11.3g.1:c.3831+11G>T | ||||||||
| F18F11.3a.1:c.3933+11G>T | ||||||||
| F18F11.3c.1:c.3831+11G>T | ||||||||
| F18F11.3d.1:c.4026+11G>T | ||||||||
| HGVSg | CHROMOSOME_IV:g.356505G>T | |||||||
| Sequence_details | SMap | S_parent | Sequence | Y66H1B | ||||
| Flanking_sequences | AGAAGCAACATCAAATTTCTGTAAGTAGTT | TCCTACACAAAACTTCTGCAACATCCAGCC | ||||||
| Mapping_target | Y66H1B | |||||||
| Source_location | 225 | CHROMOSOME_IV | 356505 | 356505 | From_analysis | Million_mutation_project_reanalysis | ||
| Type_of_mutation | Substitution | G | T | |||||
| SeqStatus | Sequenced | |||||||
| Variation_type | Natural_variant | |||||||
| Origin | Species | Caenorhabditis elegans | ||||||
| Strain | WBStrain00006622 | From_analysis | Million_mutation_project_reanalysis | |||||
| WBStrain00023072 | From_analysis | Million_mutation_project_reanalysis | ||||||
| WBStrain00027652 | From_analysis | Million_mutation_project_reanalysis | ||||||
| Laboratory | VC | |||||||
| Analysis | Million_mutation_project_reanalysis | |||||||
| Status | Live | |||||||
| Affects | Gene | WBGene00017576 | ||||||
| Transcript | F18F11.3e.1 | VEP_consequence | intron_variant | |||||
| VEP_impact | MODIFIER | |||||||
| HGVSc | F18F11.3e.1:c.3933+11G>T | |||||||
| Intron_number | 20/25 | |||||||
| F18F11.3g.1 | VEP_consequence | intron_variant | ||||||
| VEP_impact | MODIFIER | |||||||
| HGVSc | F18F11.3g.1:c.3831+11G>T | |||||||
| Intron_number | 20/25 | |||||||
| F18F11.3f.1 | VEP_consequence | intron_variant | ||||||
| VEP_impact | MODIFIER | |||||||
| HGVSc | F18F11.3f.1:c.3738+11G>T | |||||||
| Intron_number | 19/24 | |||||||
| F18F11.3h.1 | VEP_consequence | intron_variant | ||||||
| VEP_impact | MODIFIER | |||||||
| HGVSc | F18F11.3h.1:c.4026+11G>T | |||||||
| Intron_number | 21/26 | |||||||
| F18F11.3d.1 | VEP_consequence | intron_variant | ||||||
| VEP_impact | MODIFIER | |||||||
| HGVSc | F18F11.3d.1:c.4026+11G>T | |||||||
| Intron_number | 21/25 | |||||||
| F18F11.3a.1 | VEP_consequence | intron_variant | ||||||
| VEP_impact | MODIFIER | |||||||
| HGVSc | F18F11.3a.1:c.3933+11G>T | |||||||
| Intron_number | 20/25 | |||||||
| F18F11.3b.1 | VEP_consequence | intron_variant | ||||||
| VEP_impact | MODIFIER | |||||||
| HGVSc | F18F11.3b.1:c.3738+11G>T | |||||||
| Intron_number | 19/23 | |||||||
| F18F11.3c.1 | VEP_consequence | intron_variant | ||||||
| VEP_impact | MODIFIER | |||||||
| HGVSc | F18F11.3c.1:c.3831+11G>T | |||||||
| Intron_number | 20/24 | |||||||
| Method | WGS_Flibotte |
