WormBase Tree Display for Variation: WBVar01640846

WBVar01640846 Name: Public_name: WBVar01640846
    Other_name: cewivar00322961
      C09D1.1e.1:c.796-1892G>T
      C09D1.1b.1:c.796-1892G>T
      C09D1.1f.1:c.796-1892G>T
      C09D1.1l.1:c.796-1892G>T
      C09D1.1o.1:c.796-1892G>T
      C09D1.1k.1:c.796-1892G>T
      C09D1.1m.1:c.796-1892G>T
      C09D1.1n.1:c.796-1892G>T
      C09D1.1a.1:c.796-1892G>T
    HGVSg: CHROMOSOME_I:g.4042908G>T
  Sequence_details: SMap: S_parent: Sequence: C09D1
    Flanking_sequences: CGGAAGTTTTTCAGTTCACATTATTGACTT TTTCAAAATTTCATGCATTAATTATTAATC
    Mapping_target: C09D1
    Source_location: 225 CHROMOSOME_I 4042910 4042910 From_analysis: Million_mutation_project_reanalysis
    Type_of_mutation: Substitution: G T
    SeqStatus: Sequenced
  Variation_type: Natural_variant
  Origin: Species: Caenorhabditis elegans
    Strain: WBStrain00006629 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.796-1892G>T
        Intron_number: 5/48
      C09D1.1o.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: C09D1.1o.1:c.796-1892G>T
        Intron_number: 5/32
      C09D1.1k.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: C09D1.1k.1:c.796-1892G>T
        Intron_number: 5/46
      C09D1.1l.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: C09D1.1l.1:c.796-1892G>T
        Intron_number: 5/32
      C09D1.1n.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: C09D1.1n.1:c.796-1892G>T
        Intron_number: 5/46
      C09D1.1a.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: C09D1.1a.1:c.796-1892G>T
        Intron_number: 6/35
      C09D1.1e.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: C09D1.1e.1:c.796-1892G>T
        Intron_number: 5/31
      C09D1.1f.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: C09D1.1f.1:c.796-1892G>T
        Intron_number: 5/45
      C09D1.1m.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: C09D1.1m.1:c.796-1892G>T
        Intron_number: 5/47
  Method: WGS_Flibotte