WormBase Tree Display for Variation: WBVar01607001

WBVar01607001 Name: Public_name: WBVar01607001
    Other_name: cewivar00285501
      T08A11.1c.1:c.*260A>G
      T08A11.1a.1:c.*260A>G
      T08A11.1g.1:c.*260A>G
      T08A11.1d.1:c.*260A>G
      T08A11.1b.1:c.*260A>G
      T08A11.1f.1:c.*260A>G
      T08A11.1h.1:c.*260A>G
      T08A11.1e.1:c.*260A>G
    HGVSg: CHROMOSOME_III:g.4248410T>C
  Sequence_details: SMap: S_parent: Sequence: Y44F5A
    Flanking_sequences: GGGGGGAAATAAGGTTGCTTAGAAAATGTT AAAGCAACAAAAAAACATAGAATGAGAGTA
    Mapping_target: Y44F5A
    Source_location: 225 CHROMOSOME_III 4248383 4248383 From_analysis: Million_mutation_project_reanalysis
    Type_of_mutation: Substitution: T C
    SeqStatus: Sequenced
  Variation_type: Natural_variant
  Origin: Species: Caenorhabditis elegans
    Strain: WBStrain00006622 From_analysis: Million_mutation_project_reanalysis
      WBStrain00022852 From_analysis: Million_mutation_project_reanalysis
      WBStrain00022856 From_analysis: Million_mutation_project_reanalysis
      WBStrain00022878 From_analysis: Million_mutation_project_reanalysis
      WBStrain00022886 From_analysis: Million_mutation_project_reanalysis
      WBStrain00023286 From_analysis: Million_mutation_project_reanalysis
    Laboratory: VC
    Analysis: Million_mutation_project_reanalysis
    Status: Live
  Affects: Gene: WBGene00011604
    Transcript: T08A11.1e.1 VEP_consequence: 3_prime_UTR_variant
        VEP_impact: MODIFIER
        HGVSc: T08A11.1e.1:c.*260A>G
        cDNA_position: 5405
        Exon_number: 18/18
      T08A11.1g.1 VEP_consequence: 3_prime_UTR_variant
        VEP_impact: MODIFIER
        HGVSc: T08A11.1g.1:c.*260A>G
        cDNA_position: 5507
        Exon_number: 19/19
      T08A11.1h.1 VEP_consequence: 3_prime_UTR_variant
        VEP_impact: MODIFIER
        HGVSc: T08A11.1h.1:c.*260A>G
        cDNA_position: 5513
        Exon_number: 19/19
      T08A11.1d.1 VEP_consequence: 3_prime_UTR_variant
        VEP_impact: MODIFIER
        HGVSc: T08A11.1d.1:c.*260A>G
        cDNA_position: 5507
        Exon_number: 19/19
      T08A11.1f.1 VEP_consequence: 3_prime_UTR_variant
        VEP_impact: MODIFIER
        HGVSc: T08A11.1f.1:c.*260A>G
        cDNA_position: 5411
        Exon_number: 18/18
      T08A11.1c.1 VEP_consequence: 3_prime_UTR_variant
        VEP_impact: MODIFIER
        HGVSc: T08A11.1c.1:c.*260A>G
        cDNA_position: 5405
        Exon_number: 18/18
      T08A11.1b.1 VEP_consequence: 3_prime_UTR_variant
        VEP_impact: MODIFIER
        HGVSc: T08A11.1b.1:c.*260A>G
        cDNA_position: 5501
        Exon_number: 19/19
      T08A11.1a.1 VEP_consequence: 3_prime_UTR_variant
        VEP_impact: MODIFIER
        HGVSc: T08A11.1a.1:c.*260A>G
        cDNA_position: 5499
        Exon_number: 19/19
  Method: WGS_Flibotte