WormBase Tree Display for Variation: WBVar02027118

WBVar02027118 Name: Public_name: WBVar02027118
    Other_name: cewivar00755634
      C54G7.3g.1:c.2960-207_2960-206dup
      C54G7.3i.1:c.2816-207_2816-206dup
      C54G7.3f.1:c.2966-207_2966-206dup
      C54G7.3b.1:c.*243_*244dup
      C54G7.3e.1:c.3119-207_3119-206dup
      C54G7.3c.1:c.3263-207_3263-206dup
      C54G7.3a.1:c.2663-207_2663-206dup
      C54G7.3d.1:c.3110-207_3110-206dup
      C54G7.3h.1:c.2807-207_2807-206dup
    HGVSg: CHROMOSOME_X:g.5528418_5528419insTG
  Sequence_details: SMap: S_parent: Sequence: C54G7
    Flanking_sequences: CACCAGTGAGATTTTTTGAATGAAAACGTA TGTGTGTGTGTGTGTAATGATGTAATTGTG
    Mapping_target: C54G7
    Source_location: 225 CHROMOSOME_X 5528383 5528384 From_analysis: Million_mutation_project_reanalysis
    Type_of_mutation: Insertion: TG
    SeqStatus: Sequenced
  Variation_type: Natural_variant
  Origin: Species: Caenorhabditis elegans
    Strain: WBStrain00022850 From_analysis: Million_mutation_project_reanalysis
      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: WBGene00002983
    Transcript: C54G7.3i.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: C54G7.3i.1:c.2816-207_2816-206dup
        Intron_number: 18/29
      C54G7.3c.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: C54G7.3c.1:c.3263-207_3263-206dup
        Intron_number: 19/30
      C54G7.3h.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: C54G7.3h.1:c.2807-207_2807-206dup
        Intron_number: 18/29
      C54G7.3f.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: C54G7.3f.1:c.2966-207_2966-206dup
        Intron_number: 17/28
      C54G7.3d.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: C54G7.3d.1:c.3110-207_3110-206dup
        Intron_number: 18/29
      C54G7.3e.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: C54G7.3e.1:c.3119-207_3119-206dup
        Intron_number: 18/29
      C54G7.3a.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: C54G7.3a.1:c.2663-207_2663-206dup
        Intron_number: 18/30
      C54G7.3b.1 VEP_consequence: 3_prime_UTR_variant
        VEP_impact: MODIFIER
        HGVSc: C54G7.3b.1:c.*243_*244dup
        cDNA_position: 3995-3996
        Exon_number: 22/22
      C54G7.3g.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: C54G7.3g.1:c.2960-207_2960-206dup
        Intron_number: 19/30
  Method: WGS_Flibotte