WormBase Tree Display for Variation: WBVar01650477

WBVar01650477 Name: Public_name: WBVar01650477
    Other_name (11)
    HGVSg: CHROMOSOME_V:g.4501154A>C
  Sequence_details: SMap: S_parent: Sequence: T28F12
    Flanking_sequences: CATGTCAGAAGAAGAGATAAGATTTTACCC TAAATCCCTCACATATTTAGGCGCCTTTTA
    Mapping_target: T28F12
    Source_location: 225 CHROMOSOME_V 4501140 4501140 From_analysis: Million_mutation_project_reanalysis
    Type_of_mutation: Substitution: A C
    SeqStatus: Sequenced
  Variation_type: Natural_variant
  Origin: Species: Caenorhabditis elegans
    Strain: WBStrain00006629 From_analysis: Million_mutation_project_reanalysis
      WBStrain00006637 From_analysis: Million_mutation_project_reanalysis
      WBStrain00023072 From_analysis: Million_mutation_project_reanalysis
      WBStrain00023139 From_analysis: Million_mutation_project_reanalysis
      WBStrain00023191 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: WBGene00006796
    Transcript: T28F12.2e.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: T28F12.2e.1:c.13-65A>C
        Intron_number: 1/9
      T28F12.2d.4 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: T28F12.2d.4:c.-1224-65A>C
        Intron_number: 1/11
      T28F12.2d.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: T28F12.2d.1:c.-1224-65A>C
        Intron_number: 1/11
      T28F12.2a.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: T28F12.2a.1:c.124-65A>C
        Intron_number: 2/11
      T28F12.2b.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: T28F12.2b.1:c.13-65A>C
        Intron_number: 2/11
      T28F12.2d.2 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: T28F12.2d.2:c.-1242-65A>C
        Intron_number: 1/11
      T28F12.2c.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: T28F12.2c.1:c.-1806-65A>C
        Intron_number: 1/10
      T28F12.2d.3 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: T28F12.2d.3:c.-1242-65A>C
        Intron_number: 1/11
      T28F12.2c.2 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: T28F12.2c.2:c.-1422-65A>C
        Intron_number: 1/10
      T28F12.2f.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: T28F12.2f.1:c.124-65A>C
        Intron_number: 2/10
  Method: WGS_Flibotte