WormBase Tree Display for Variation: WBVar02052732

WBVar02052732 Name: Public_name: WBVar02052732
    Other_name: cewivar00781932
      C09D1.1m.1:c.795+1146_795+1147insT
      C09D1.1l.1:c.795+1146_795+1147insT
      C09D1.1e.1:c.795+1146_795+1147insT
      C09D1.1o.1:c.795+1146_795+1147insT
      C09D1.1b.1:c.795+1146_795+1147insT
      C09D1.1n.1:c.795+1146_795+1147insT
      C09D1.1a.1:c.795+1146_795+1147insT
      C09D1.1f.1:c.795+1146_795+1147insT
      C09D1.1k.1:c.795+1146_795+1147insT
    HGVSg: CHROMOSOME_I:g.4040018_4040019insT
  Sequence_details: SMap: S_parent: Sequence: C09D1
    Flanking_sequences: TATTCAATCTTTTCCACTGAGTTCTGAGTA TTTTTTTTTCAAAAAGCCAGCTAGCGCTAT
    Mapping_target: C09D1
    Source_location: 225 CHROMOSOME_I 4040020 4040021 From_analysis: Million_mutation_project_reanalysis
    Type_of_mutation: Insertion: T
    SeqStatus: Sequenced
  Variation_type: Natural_variant
  Origin: Species: Caenorhabditis elegans
    Strain: WBStrain00022930 From_analysis: Million_mutation_project_reanalysis
    Laboratory: VC
    Analysis: Million_mutation_project_reanalysis
    Status: Live
  Affects: Gene: WBGene00006820
    Transcript: C09D1.1b.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: C09D1.1b.1:c.795+1146_795+1147insT
        Intron_number: 5/48
      C09D1.1o.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: C09D1.1o.1:c.795+1146_795+1147insT
        Intron_number: 5/32
      C09D1.1k.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: C09D1.1k.1:c.795+1146_795+1147insT
        Intron_number: 5/46
      C09D1.1l.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: C09D1.1l.1:c.795+1146_795+1147insT
        Intron_number: 5/32
      C09D1.1n.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: C09D1.1n.1:c.795+1146_795+1147insT
        Intron_number: 5/46
      C09D1.1a.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: C09D1.1a.1:c.795+1146_795+1147insT
        Intron_number: 6/35
      C09D1.1e.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: C09D1.1e.1:c.795+1146_795+1147insT
        Intron_number: 5/31
      C09D1.1f.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: C09D1.1f.1:c.795+1146_795+1147insT
        Intron_number: 5/45
      C09D1.1m.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: C09D1.1m.1:c.795+1146_795+1147insT
        Intron_number: 5/47
  Method: WGS_Flibotte