WormBase Tree Display for Variation: WBVar02027438

WBVar02027438 Name: Public_name: WBVar02027438
    Other_name: cewivar00755956
      C34E11.t1.1:n.55_61del
      C34E11.2b.1:c.1686-104_1686-98del
      C34E11.2a.1:c.1953-104_1953-98del
      C34E11.2c.1:c.1854-104_1854-98del
      C34E11.2f.1:c.1714-104_1714-98del
      C34E11.2g.1:c.1628-104_1628-98del
      C34E11.2e.1:c.1996-104_1996-98del
      C34E11.2d.1:c.1671-104_1671-98del
    HGVSg: CHROMOSOME_X:g.11806600_11806606del
  Sequence_details: SMap: S_parent: Sequence: C34E11
    Flanking_sequences: AAAATTGAGAAAAAATGTCGACCACGGCAG ACCTGTAATCCCCAGATTCGAAGTCTGGTG
    Mapping_target: C34E11
    Source_location: 225 CHROMOSOME_X 11806532 11806538 From_analysis: Million_mutation_project_reanalysis
    Type_of_mutation: Deletion
    SeqStatus: Sequenced
  Variation_type: Natural_variant
  Origin: Species: Caenorhabditis elegans
    Strain: WBStrain00023139 From_analysis: Million_mutation_project_reanalysis
      WBStrain00027648 From_analysis: Million_mutation_project_reanalysis
      WBStrain00027660 From_analysis: Million_mutation_project_reanalysis
    Laboratory: VC
    Analysis: Million_mutation_project_reanalysis
    Status: Live
  Affects: Gene: WBGene00014276
      WBGene00007935
    Transcript: C34E11.t1 VEP_consequence: non_coding_transcript_exon_variant
        VEP_impact: MODIFIER
        HGVSc: C34E11.t1.1:n.55_61del
        cDNA_position: 55-61
        Exon_number: 1/1
      C34E11.2a.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: C34E11.2a.1:c.1953-104_1953-98del
        Intron_number: 13/15
      C34E11.2f.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: C34E11.2f.1:c.1714-104_1714-98del
        Intron_number: 14/15
      C34E11.2e.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: C34E11.2e.1:c.1996-104_1996-98del
        Intron_number: 14/15
      C34E11.2c.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: C34E11.2c.1:c.1854-104_1854-98del
        Intron_number: 12/13
      C34E11.2b.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: C34E11.2b.1:c.1686-104_1686-98del
        Intron_number: 11/12
      C34E11.2g.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: C34E11.2g.1:c.1628-104_1628-98del
        Intron_number: 11/12
      C34E11.2d.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: C34E11.2d.1:c.1671-104_1671-98del
        Intron_number: 12/14
  Method: WGS_Flibotte