WormBase Tree Display for Variation: WBVar02039834

WBVar02039834 Name: Public_name: WBVar02039834
    Other_name: cewivar00768631
      Y43H11AL.1d.1:c.108+262_108+265del
      Y43H11AL.1a.3:c.1083+262_1083+265del
      Y43H11AL.1c.1:c.1041+262_1041+265del
      Y43H11AL.1a.2:c.1083+262_1083+265del
      Y43H11AL.1a.4:c.1083+262_1083+265del
      Y43H11AL.1b.1:c.1083+262_1083+265del
      Y43H11AL.1a.1:c.1083+262_1083+265del
    HGVSg: CHROMOSOME_II:g.227671_227674del
  Sequence_details: SMap: S_parent: Sequence: Y43H11AL
    Flanking_sequences: GACCAATTTTTCCAAAACTTTGAGCGGCCA TTTTTTTGGTGAAATTGAAATTTTCAGAGC
    Mapping_target: Y43H11AL
    Source_location: 225 CHROMOSOME_II 227671 227674 From_analysis: Million_mutation_project_reanalysis
    Type_of_mutation: Deletion
    SeqStatus: Sequenced
  Variation_type: Natural_variant
  Origin: Species: Caenorhabditis elegans
    Strain: WBStrain00022850 From_analysis: Million_mutation_project_reanalysis
      WBStrain00023018 From_analysis: Million_mutation_project_reanalysis
    Laboratory: VC
    Analysis: Million_mutation_project_reanalysis
    Status: Live
  Affects: Gene: WBGene00021545
    Transcript: Y43H11AL.1a.3 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: Y43H11AL.1a.3:c.1083+262_1083+265del
        Intron_number: 7/10
      Y43H11AL.1c.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: Y43H11AL.1c.1:c.1041+262_1041+265del
        Intron_number: 5/8
      Y43H11AL.1d.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: Y43H11AL.1d.1:c.108+262_108+265del
        Intron_number: 1/4
      Y43H11AL.1b.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: Y43H11AL.1b.1:c.1083+262_1083+265del
        Intron_number: 7/11
      Y43H11AL.1a.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: Y43H11AL.1a.1:c.1083+262_1083+265del
        Intron_number: 7/10
      Y43H11AL.1a.2 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: Y43H11AL.1a.2:c.1083+262_1083+265del
        Intron_number: 7/8
      Y43H11AL.1a.4 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: Y43H11AL.1a.4:c.1083+262_1083+265del
        Intron_number: 7/9
  Method: WGS_Flibotte