WormBase Tree Display for Variation: WBVar01994980

WBVar01994980 Name: Public_name: WBVar01994980
    Other_name: cewivar00722274
      B0285.1c.2:c.1365-8_1365-7insTT
      B0285.1c.1:c.1365-8_1365-7insTT
      B0285.1b.2:c.1365-8_1365-7insTT
      B0285.1b.1:c.1365-8_1365-7insTT
      B0285.1a.2:c.1365-8_1365-7insTT
      B0285.1a.1:c.1365-8_1365-7insTT
    HGVSg: CHROMOSOME_III:g.4338406_4338407insTT
  Sequence_details: SMap: S_parent: Sequence: B0285
    Flanking_sequences: CAATCAGAACTTTAATAATTTTGAAAATTG TTTGCAGAGGCGAGCTGAAGATTGCTGATC
    Mapping_target: B0285
    Source_location: 225 CHROMOSOME_III 4338379 4338380 From_analysis: Million_mutation_project_reanalysis
    Type_of_mutation: Insertion: TT
    SeqStatus: Sequenced
  Variation_type: Natural_variant
  Origin: Species: Caenorhabditis elegans
    Strain: WBStrain00006629 From_analysis: Million_mutation_project_reanalysis
      WBStrain00006637 From_analysis: Million_mutation_project_reanalysis
      WBStrain00023018 From_analysis: Million_mutation_project_reanalysis
      WBStrain00023072 From_analysis: Million_mutation_project_reanalysis
      WBStrain00023191 From_analysis: Million_mutation_project_reanalysis
      WBStrain00024204 From_analysis: Million_mutation_project_reanalysis
    Laboratory: VC
    Analysis: Million_mutation_project_reanalysis
    Status: Live
  Affects: Gene: WBGene00007135
    Transcript: B0285.1c.2 VEP_consequence: splice_region_variant,intron_variant
        VEP_impact: LOW
        HGVSc: B0285.1c.2:c.1365-8_1365-7insTT
        Intron_number: 9/14
      B0285.1b.2 VEP_consequence: splice_region_variant,intron_variant
        VEP_impact: LOW
        HGVSc: B0285.1b.2:c.1365-8_1365-7insTT
        Intron_number: 9/14
      B0285.1c.1 VEP_consequence: splice_region_variant,intron_variant
        VEP_impact: LOW
        HGVSc: B0285.1c.1:c.1365-8_1365-7insTT
        Intron_number: 11/16
      B0285.1a.2 VEP_consequence: splice_region_variant,intron_variant
        VEP_impact: LOW
        HGVSc: B0285.1a.2:c.1365-8_1365-7insTT
        Intron_number: 9/14
      B0285.1b.1 VEP_consequence: splice_region_variant,intron_variant
        VEP_impact: LOW
        HGVSc: B0285.1b.1:c.1365-8_1365-7insTT
        Intron_number: 11/16
      B0285.1a.1 VEP_consequence: splice_region_variant,intron_variant
        VEP_impact: LOW
        HGVSc: B0285.1a.1:c.1365-8_1365-7insTT
        Intron_number: 11/16
  Method: WGS_Flibotte