WormBase Tree Display for Variation: WBVar01710869
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WBVar01710869 | Name | Public_name | WBVar01710869 | |||||
---|---|---|---|---|---|---|---|---|
Other_name | cewivar00408536 | |||||||
F43C9.2b.1:c.298+155T>C | ||||||||
F43C9.9:n.59A>G | ||||||||
F43C9.2a.1:c.343+155T>C | ||||||||
HGVSg | CHROMOSOME_X:g.4789783T>C | |||||||
Sequence_details | SMap | S_parent | Sequence | F43C9 | ||||
Flanking_sequences | CGGTCTCCCAAAGTTCATTTTATTTCATTG | GCAGAAGGAGAGCCAGCGAGCGAGCAAAGC | ||||||
Mapping_target | F43C9 | |||||||
Source_location | 225 | CHROMOSOME_X | 4789753 | 4789753 | From_analysis | Million_mutation_project_reanalysis | ||
Type_of_mutation | Substitution | T | C | |||||
SeqStatus | Sequenced | |||||||
Variation_type | Natural_variant | |||||||
Origin | Species | Caenorhabditis elegans | ||||||
Strain | WBStrain00022850 | From_analysis | Million_mutation_project_reanalysis | |||||
WBStrain00022852 | From_analysis | Million_mutation_project_reanalysis | ||||||
WBStrain00022856 | From_analysis | Million_mutation_project_reanalysis | ||||||
WBStrain00022878 | From_analysis | Million_mutation_project_reanalysis | ||||||
WBStrain00022886 | From_analysis | Million_mutation_project_reanalysis | ||||||
WBStrain00022902 | From_analysis | Million_mutation_project_reanalysis | ||||||
WBStrain00023138 | 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 | ||||||
Laboratory | VC | |||||||
Analysis | Million_mutation_project_reanalysis | |||||||
Status | Live | |||||||
Affects | Gene | WBGene00018376 | ||||||
WBGene00202168 | ||||||||
Transcript | F43C9.2a.1 | VEP_consequence | intron_variant | |||||
VEP_impact | MODIFIER | |||||||
HGVSc | F43C9.2a.1:c.343+155T>C | |||||||
Intron_number | 4/5 | |||||||
F43C9.9 | VEP_consequence | non_coding_transcript_exon_variant | ||||||
VEP_impact | MODIFIER | |||||||
HGVSc | F43C9.9:n.59A>G | |||||||
cDNA_position | 59 | |||||||
Exon_number | 1/1 | |||||||
F43C9.2b.1 | VEP_consequence | intron_variant | ||||||
VEP_impact | MODIFIER | |||||||
HGVSc | F43C9.2b.1:c.298+155T>C | |||||||
Intron_number | 4/5 | |||||||
Method | WGS_Flibotte |