WormBase Tree Display for Variation: WBVar01786385

WBVar01786385 Name: Public_name: WBVar01786385
    Other_name (14)
    HGVSg: CHROMOSOME_IV:g.6171640A>G
  Sequence_details: SMap: S_parent: Sequence: C11D2
    Flanking_sequences: TTTGATATGTGTGAGAAAAACTGACTTGCA TTGAAAAAATTATGTAATTCGATCTCCCCC
    Mapping_target: C11D2
    Source_location: 225 CHROMOSOME_IV 6171629 6171629 From_analysis: Million_mutation_project_reanalysis
    Type_of_mutation: Substitution: A G
    SeqStatus: Sequenced
  Variation_type: Natural_variant
  Origin: Species: Caenorhabditis elegans
    Strain: WBStrain00023192 From_analysis: Million_mutation_project_reanalysis
    Laboratory: VC
    Analysis: Million_mutation_project_reanalysis
    Status: Live
  Affects: Gene: WBGene00201142
      WBGene00006809
    Transcript: C11D2.6o.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: C11D2.6o.1:c.80-234T>C
        Intron_number: 2/28
      C11D2.6p.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: C11D2.6p.1:c.80-234T>C
        Intron_number: 2/28
      C11D2.6i.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: C11D2.6i.1:c.26-234T>C
        Intron_number: 1/28
      C11D2.6a.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: C11D2.6a.1:c.62-234T>C
        Intron_number: 2/29
      C11D2.100 VEP_consequence: non_coding_transcript_exon_variant
        VEP_impact: MODIFIER
        HGVSc: C11D2.100:n.53A>G
        cDNA_position: 53
        Exon_number: 1/1
      C11D2.6l.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: C11D2.6l.1:c.26-234T>C
        Intron_number: 1/27
      C11D2.6d.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: C11D2.6d.1:c.62-234T>C
        Intron_number: 1/28
      C11D2.6e.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: C11D2.6e.1:c.62-234T>C
        Intron_number: 1/27
      C11D2.6n.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: C11D2.6n.1:c.80-234T>C
        Intron_number: 2/27
      C11D2.6g.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: C11D2.6g.1:c.62-234T>C
        Intron_number: 1/27
      C11D2.6m.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: C11D2.6m.1:c.80-234T>C
        Intron_number: 2/29
      C11D2.6j.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: C11D2.6j.1:c.26-234T>C
        Intron_number: 1/26
      C11D2.6k.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: C11D2.6k.1:c.26-234T>C
        Intron_number: 1/27
  Method: WGS_Flibotte