WormBase Tree Display for Variation: WBVar01990796

WBVar01990796 Name: Public_name: WBVar01990796
    Other_name (11)
    HGVSg: CHROMOSOME_IV:g.4015076_4015077insT
  Sequence_details: SMap: S_parent: Sequence: W02C12
    Flanking_sequences: GGGGGGCCTAGAAACAGGGAACATCATTTA TTTTTTGGGGGATTTTTTGAATGTTTCTTT
    Mapping_target: W02C12
    Source_location: 225 CHROMOSOME_IV 4015070 4015071 From_analysis: Million_mutation_project_reanalysis
    Type_of_mutation: Insertion: T
    SeqStatus: Sequenced
  Variation_type: Natural_variant
  Origin: Species: Caenorhabditis elegans
    Strain: WBStrain00006625 From_analysis: Million_mutation_project_reanalysis
      WBStrain00023139 From_analysis: Million_mutation_project_reanalysis
      WBStrain00023192 From_analysis: Million_mutation_project_reanalysis
      WBStrain00027648 From_analysis: Million_mutation_project_reanalysis
      WBStrain00027652 From_analysis: Million_mutation_project_reanalysis
      WBStrain00027660 From_analysis: Million_mutation_project_reanalysis
      WBStrain00027662 From_analysis: Million_mutation_project_reanalysis
    Laboratory: VC
    Analysis: Million_mutation_project_reanalysis
    Status: Live
  Affects: Gene: WBGene00020930
    Transcript: W02C12.3e.1 VEP_consequence: 3_prime_UTR_variant
        VEP_impact: MODIFIER
        HGVSc: W02C12.3e.1:c.*682dup
        cDNA_position: 2002-2003
        Exon_number: 10/10
      W02C12.3d.1 VEP_consequence: 3_prime_UTR_variant
        VEP_impact: MODIFIER
        HGVSc: W02C12.3d.1:c.*682dup
        cDNA_position: 2077-2078
        Exon_number: 11/11
      W02C12.3g.1 VEP_consequence: 3_prime_UTR_variant
        VEP_impact: MODIFIER
        HGVSc: W02C12.3g.1:c.*930dup
        cDNA_position: 2306-2307
        Exon_number: 11/11
      W02C12.3c.1 VEP_consequence: 3_prime_UTR_variant
        VEP_impact: MODIFIER
        HGVSc: W02C12.3c.1:c.*682dup
        cDNA_position: 2298-2299
        Exon_number: 13/13
      W02C12.3h.2 VEP_consequence: 3_prime_UTR_variant
        VEP_impact: MODIFIER
        HGVSc: W02C12.3h.2:c.*682dup
        cDNA_position: 1871-1872
        Exon_number: 10/10
      W02C12.3a.1 VEP_consequence: 3_prime_UTR_variant
        VEP_impact: MODIFIER
        HGVSc: W02C12.3a.1:c.*682dup
        cDNA_position: 2240-2241
        Exon_number: 12/12
      W02C12.3f.1 VEP_consequence: 3_prime_UTR_variant
        VEP_impact: MODIFIER
        HGVSc: W02C12.3f.1:c.*682dup
        cDNA_position: 2167-2168
        Exon_number: 11/11
      W02C12.3a.2 VEP_consequence: 3_prime_UTR_variant
        VEP_impact: MODIFIER
        HGVSc: W02C12.3a.2:c.*682dup
        cDNA_position: 2237-2238
        Exon_number: 12/12
      W02C12.3b.1 VEP_consequence: 3_prime_UTR_variant
        VEP_impact: MODIFIER
        HGVSc: W02C12.3b.1:c.*682dup
        cDNA_position: 2223-2224
        Exon_number: 12/12
      W02C12.3d.2 VEP_consequence: 3_prime_UTR_variant
        VEP_impact: MODIFIER
        HGVSc: W02C12.3d.2:c.*682dup
        cDNA_position: 2271-2272
        Exon_number: 12/12
  Method: WGS_Flibotte