WormBase Tree Display for Variation: WBVar01514943

WBVar01514943 Name: Public_name: WBVar01514943
    Other_name: cewivar00037809
      B0212.5.1:c.2397+55T>C
      B0212.7:n.174A>G
    HGVSg: CHROMOSOME_IV:g.3552302A>G
  Sequence_details: SMap: S_parent: Sequence: B0212
    Flanking_sequences: CTGCCGTTACTAGTCGCTAAAAAAAACTAG CACCCTGCCCCTCTCCCAGCTGACTCTCGT
    Mapping_target: B0212
    Source_location: 225 CHROMOSOME_IV 3552298 3552298 From_analysis: Million_mutation_project_reanalysis
    Type_of_mutation: Substitution: A G
    SeqStatus: Sequenced
  Variation_type: Natural_variant
  Origin: Species: Caenorhabditis elegans
    Strain: WBStrain00000032 From_analysis: Million_mutation_project_reanalysis
      WBStrain00022883 From_analysis: Million_mutation_project_reanalysis
      WBStrain00022887 From_analysis: Million_mutation_project_reanalysis
      WBStrain00022930 From_analysis: Million_mutation_project_reanalysis
      WBStrain00023139 From_analysis: Million_mutation_project_reanalysis
      WBStrain00023286 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: WBGene00200460
      WBGene00003889
    Transcript: B0212.5.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: B0212.5.1:c.2397+55T>C
        Intron_number: 12/14
      B0212.7 VEP_consequence: non_coding_transcript_exon_variant
        VEP_impact: MODIFIER
        HGVSc: B0212.7:n.174A>G
        cDNA_position: 174
        Exon_number: 1/1
  Method: WGS_Flibotte