WormBase Tree Display for Variation: WBVar01626322
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WBVar01626322 | Name | Public_name | WBVar01626322 | |||||
---|---|---|---|---|---|---|---|---|
Other_name | cewivar00306459 | |||||||
F53C3.13f.1:c.855-87T>A | ||||||||
F53C3.13a.1:c.849-87T>A | ||||||||
F53C3.13d.1:c.849-87T>A | ||||||||
F53C3.13e.1:c.849-87T>A | ||||||||
F53C3.13b.1:c.849-87T>A | ||||||||
F53C3.13d.2:c.849-87T>A | ||||||||
F53C3.13c.1:c.849-87T>A | ||||||||
HGVSg | CHROMOSOME_II:g.3924655A>T | |||||||
Sequence_details | SMap | S_parent | Sequence | F53C3 | ||||
Flanking_sequences | ATTGAAAATTTCCAATTTTTTCGAATAATT | AAAAAAAAGACACACATTTTCTGAAAAACT | ||||||
Mapping_target | F53C3 | |||||||
Source_location | 225 | CHROMOSOME_II | 3924657 | 3924657 | From_analysis | Million_mutation_project_reanalysis | ||
Type_of_mutation | Substitution | A | T | |||||
SeqStatus | Sequenced | |||||||
Variation_type | Natural_variant | |||||||
Origin | Species | Caenorhabditis elegans | ||||||
Strain (11) | ||||||||
Laboratory | VC | |||||||
Analysis | Million_mutation_project_reanalysis | |||||||
Status | Live | |||||||
Affects | Gene | WBGene00018756 | ||||||
Transcript | F53C3.13e.1 | VEP_consequence | intron_variant | |||||
VEP_impact | MODIFIER | |||||||
HGVSc | F53C3.13e.1:c.849-87T>A | |||||||
Intron_number | 4/6 | |||||||
F53C3.13b.1 | VEP_consequence | intron_variant | ||||||
VEP_impact | MODIFIER | |||||||
HGVSc | F53C3.13b.1:c.849-87T>A | |||||||
Intron_number | 4/6 | |||||||
F53C3.13d.1 | VEP_consequence | intron_variant | ||||||
VEP_impact | MODIFIER | |||||||
HGVSc | F53C3.13d.1:c.849-87T>A | |||||||
Intron_number | 4/7 | |||||||
F53C3.13a.1 | VEP_consequence | intron_variant | ||||||
VEP_impact | MODIFIER | |||||||
HGVSc | F53C3.13a.1:c.849-87T>A | |||||||
Intron_number | 4/6 | |||||||
F53C3.13d.2 | VEP_consequence | intron_variant | ||||||
VEP_impact | MODIFIER | |||||||
HGVSc | F53C3.13d.2:c.849-87T>A | |||||||
Intron_number | 4/6 | |||||||
F53C3.13f.1 | VEP_consequence | intron_variant | ||||||
VEP_impact | MODIFIER | |||||||
HGVSc | F53C3.13f.1:c.855-87T>A | |||||||
Intron_number | 4/6 | |||||||
F53C3.13c.1 | VEP_consequence | intron_variant | ||||||
VEP_impact | MODIFIER | |||||||
HGVSc | F53C3.13c.1:c.849-87T>A | |||||||
Intron_number | 4/6 | |||||||
Method | WGS_Flibotte |