WormBase Tree Display for Variation: WBVar01980961

WBVar01980961 Name: Public_name: WBVar01980961
    Other_name: cewivar00707044
      C47C12.6g.1:c.1918-169_1918-168insA
      C47C12.6f.1:c.1924-169_1924-168insA
      C47C12.6b.1:c.2176-169_2176-168insA
      C47C12.6d.1:c.1954-169_1954-168insA
      C47C12.6a.1:c.1978-169_1978-168insA
      C47C12.6a.2:c.1978-169_1978-168insA
      C47C12.6c.1:c.2008-169_2008-168insA
      C47C12.6e.1:c.2146-169_2146-168insA
    HGVSg: CHROMOSOME_X:g.7767810_7767811insA
  Sequence_details: SMap: S_parent: Sequence: C47C12
    Flanking_sequences: TTTTCGTAGAGTATCAATGTTTTCATTTTG AAAAAAAAAGGTGCATTTGTATATTCTTAA
    Mapping_target: C47C12
    Source_location: 225 CHROMOSOME_X 7767759 7767760 From_analysis: Million_mutation_project_reanalysis
    Type_of_mutation: Insertion: A
    SeqStatus: Sequenced
  Variation_type: Natural_variant
  Origin: Species: Caenorhabditis elegans
    Strain: WBStrain00004602 From_analysis: Million_mutation_project_reanalysis
    Laboratory: VC
    Analysis: Million_mutation_project_reanalysis
    Status: Live
  Affects: Gene: WBGene00000950
    Transcript: C47C12.6e.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: C47C12.6e.1:c.2146-169_2146-168insA
        Intron_number: 14/16
      C47C12.6c.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: C47C12.6c.1:c.2008-169_2008-168insA
        Intron_number: 14/16
      C47C12.6a.2 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: C47C12.6a.2:c.1978-169_1978-168insA
        Intron_number: 13/16
      C47C12.6b.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: C47C12.6b.1:c.2176-169_2176-168insA
        Intron_number: 15/17
      C47C12.6a.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: C47C12.6a.1:c.1978-169_1978-168insA
        Intron_number: 14/17
      C47C12.6d.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: C47C12.6d.1:c.1954-169_1954-168insA
        Intron_number: 13/15
      C47C12.6f.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: C47C12.6f.1:c.1924-169_1924-168insA
        Intron_number: 12/14
      C47C12.6g.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: C47C12.6g.1:c.1918-169_1918-168insA
        Intron_number: 16/18
  Method: WGS_Flibotte