WormBase Tree Display for Variation: WBVar01590438
expand all nodes | collapse all nodes | view schema
WBVar01590438 | Name | Public_name | WBVar01590438 | |||||
---|---|---|---|---|---|---|---|---|
Other_name | cewivar00244166 | |||||||
ZC376.7c.2:c.496-471A>T | ||||||||
ZC376.7b.1:c.496-471A>T | ||||||||
ZC376.7b.2:c.496-471A>T | ||||||||
ZC376.7a.1:c.544-471A>T | ||||||||
ZC376.7c.1:c.496-471A>T | ||||||||
ZC376.7a.2:c.544-471A>T | ||||||||
HGVSg | CHROMOSOME_V:g.14195744A>T | |||||||
Sequence_details | SMap | S_parent | Sequence | ZC376 | ||||
Flanking_sequences | TTTTTCAGACACTTTTTCGGTTATCAAGTT | TCTTCACGGAAAAATGTTCGAAAAATTGGC | ||||||
Mapping_target | ZC376 | |||||||
Source_location | 225 | CHROMOSOME_V | 14195729 | 14195729 | From_analysis | Million_mutation_project_reanalysis | ||
Type_of_mutation | Substitution | A | T | |||||
SeqStatus | Sequenced | |||||||
Variation_type | Natural_variant | |||||||
Origin | Species | Caenorhabditis elegans | ||||||
Strain | WBStrain00004602 | From_analysis | Million_mutation_project_reanalysis | |||||
WBStrain00022850 | From_analysis | Million_mutation_project_reanalysis | ||||||
WBStrain00022930 | 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 | WBGene00013878 | ||||||
Transcript | ZC376.7c.1 | VEP_consequence | intron_variant | |||||
VEP_impact | MODIFIER | |||||||
HGVSc | ZC376.7c.1:c.496-471A>T | |||||||
Intron_number | 5/9 | |||||||
ZC376.7a.2 | VEP_consequence | intron_variant | ||||||
VEP_impact | MODIFIER | |||||||
HGVSc | ZC376.7a.2:c.544-471A>T | |||||||
Intron_number | 5/9 | |||||||
ZC376.7b.2 | VEP_consequence | intron_variant | ||||||
VEP_impact | MODIFIER | |||||||
HGVSc | ZC376.7b.2:c.496-471A>T | |||||||
Intron_number | 6/10 | |||||||
ZC376.7a.1 | VEP_consequence | intron_variant | ||||||
VEP_impact | MODIFIER | |||||||
HGVSc | ZC376.7a.1:c.544-471A>T | |||||||
Intron_number | 4/8 | |||||||
ZC376.7c.2 | VEP_consequence | intron_variant | ||||||
VEP_impact | MODIFIER | |||||||
HGVSc | ZC376.7c.2:c.496-471A>T | |||||||
Intron_number | 6/10 | |||||||
ZC376.7b.1 | VEP_consequence | intron_variant | ||||||
VEP_impact | MODIFIER | |||||||
HGVSc | ZC376.7b.1:c.496-471A>T | |||||||
Intron_number | 5/9 | |||||||
Method | WGS_Flibotte |