WormBase Tree Display for Variation: WBVar01784511

WBVar01784511 Name: Public_name: WBVar01784511
    Other_name: cewivar00485627
      F45E10.1a.1:c.1971-1059A>G
      F45E10.1h.1:c.1971-1059A>G
      F45E10.1e.1:c.711-1059A>G
      F45E10.1d.1:c.1569-1059A>G
      F45E10.1g.1:c.1971-1059A>G
      F45E10.1c.1:c.1971-1059A>G
      F45E10.1f.1:c.1047-1059A>G
      F45E10.1b.1:c.1971-1059A>G
    HGVSg: CHROMOSOME_II:g.11064553T>C
  Sequence_details: SMap: S_parent: Sequence: F45E10
    Flanking_sequences: GAGAGCGGGGGACGCGCAGGACACACAGTT AGTTATTTATGAGGAAGAGGGAGAAAGATT
    Mapping_target: F45E10
    Source_location: 225 CHROMOSOME_II 11064495 11064495 From_analysis: Million_mutation_project_reanalysis
    Type_of_mutation: Substitution: T C
    SeqStatus: Sequenced
  Variation_type: Natural_variant
  Origin: Species: Caenorhabditis elegans
    Strain: WBStrain00022886 From_analysis: Million_mutation_project_reanalysis
      WBStrain00023018 From_analysis: Million_mutation_project_reanalysis
      WBStrain00023192 From_analysis: Million_mutation_project_reanalysis
      WBStrain00023286 From_analysis: Million_mutation_project_reanalysis
    Laboratory: VC
    Analysis: Million_mutation_project_reanalysis
    Status: Live
  Affects: Gene: WBGene00006788
    Transcript: F45E10.1b.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: F45E10.1b.1:c.1971-1059A>G
        Intron_number: 14/22
      F45E10.1a.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: F45E10.1a.1:c.1971-1059A>G
        Intron_number: 15/23
      F45E10.1f.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: F45E10.1f.1:c.1047-1059A>G
        Intron_number: 7/15
      F45E10.1c.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: F45E10.1c.1:c.1971-1059A>G
        Intron_number: 14/23
      F45E10.1e.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: F45E10.1e.1:c.711-1059A>G
        Intron_number: 6/14
      F45E10.1d.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: F45E10.1d.1:c.1569-1059A>G
        Intron_number: 12/20
      F45E10.1g.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: F45E10.1g.1:c.1971-1059A>G
        Intron_number: 14/21
      F45E10.1h.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: F45E10.1h.1:c.1971-1059A>G
        Intron_number: 14/21
  Method: WGS_Flibotte