WormBase Tree Display for Variation: WBVar01616284
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WBVar01616284 | Name | Public_name | WBVar01616284 | |||||
---|---|---|---|---|---|---|---|---|
Other_name | cewivar00295771 | |||||||
W08A12.1b.1:c.142-1751T>C | ||||||||
W08A12.1c.1:c.124-1751T>C | ||||||||
W08A12.1b.2:c.142-1751T>C | ||||||||
W08A12.1a.1:c.48-270T>C | ||||||||
W08A12.1b.3:c.142-1751T>C | ||||||||
W08A12.1e.1:c.67-1751T>C | ||||||||
HGVSg | CHROMOSOME_V:g.3695701T>C | |||||||
Sequence_details | SMap | S_parent | Sequence | W08A12 | ||||
Flanking_sequences | GCCTAGAGGGCTTTTCTTTGATTAATAAGA | AAGCGCATTTTCGGAAATTGAATTAGTCGG | ||||||
Mapping_target | W08A12 | |||||||
Source_location | 225 | CHROMOSOME_V | 3695688 | 3695688 | From_analysis | Million_mutation_project_reanalysis | ||
Type_of_mutation | Substitution | T | C | |||||
SeqStatus | Sequenced | |||||||
Variation_type | Natural_variant | |||||||
Origin | Species | Caenorhabditis elegans | ||||||
Strain | WBStrain00006622 | From_analysis | Million_mutation_project_reanalysis | |||||
WBStrain00022930 | From_analysis | Million_mutation_project_reanalysis | ||||||
WBStrain00023072 | From_analysis | Million_mutation_project_reanalysis | ||||||
Laboratory | VC | |||||||
Analysis | Million_mutation_project_reanalysis | |||||||
Status | Live | |||||||
Affects | Gene | WBGene00021078 | ||||||
Transcript | W08A12.1b.3 | VEP_consequence | intron_variant | |||||
VEP_impact | MODIFIER | |||||||
HGVSc | W08A12.1b.3:c.142-1751T>C | |||||||
Intron_number | 3/7 | |||||||
W08A12.1a.1 | VEP_consequence | intron_variant | ||||||
VEP_impact | MODIFIER | |||||||
HGVSc | W08A12.1a.1:c.48-270T>C | |||||||
Intron_number | 2/7 | |||||||
W08A12.1c.1 | VEP_consequence | intron_variant | ||||||
VEP_impact | MODIFIER | |||||||
HGVSc | W08A12.1c.1:c.124-1751T>C | |||||||
Intron_number | 3/7 | |||||||
W08A12.1b.2 | VEP_consequence | intron_variant | ||||||
VEP_impact | MODIFIER | |||||||
HGVSc | W08A12.1b.2:c.142-1751T>C | |||||||
Intron_number | 4/8 | |||||||
W08A12.1b.1 | VEP_consequence | intron_variant | ||||||
VEP_impact | MODIFIER | |||||||
HGVSc | W08A12.1b.1:c.142-1751T>C | |||||||
Intron_number | 4/8 | |||||||
W08A12.1e.1 | VEP_consequence | intron_variant | ||||||
VEP_impact | MODIFIER | |||||||
HGVSc | W08A12.1e.1:c.67-1751T>C | |||||||
Intron_number | 1/4 | |||||||
Method | WGS_Flibotte |