WormBase Tree Display for Variation: WBVar01559646

WBVar01559646 Name: Public_name: WBVar01559646
    Other_name: cewivar00139915
      T24H10.7h.1:c.509+2300T>C
      T24H10.7b.1:c.647+2300T>C
      T24H10.7f.1:c.551+2300T>C
      T24H10.7g.1:c.275+2300T>C
      T24H10.7a.1:c.707+2300T>C
      T24H10.7i.1:c.398+2300T>C
    HGVSg: CHROMOSOME_II:g.9125636T>C
  Sequence_details: SMap: S_parent: Sequence: T24H10
    Flanking_sequences: TGATTTCTTGAACAGATGAGGTCTGCATTT TTATTTTTTTTTTAAGCTTGTCCAAAATTT
    Mapping_target: T24H10
    Source_location: 225 CHROMOSOME_II 9125574 9125574 From_analysis: Million_mutation_project_reanalysis
    Type_of_mutation: Substitution: T C
    SeqStatus: Sequenced
  Variation_type: Natural_variant
  Origin: Species: Caenorhabditis elegans
    Strain: WBStrain00004600 From_analysis: Million_mutation_project_reanalysis
      WBStrain00006629 From_analysis: Million_mutation_project_reanalysis
      WBStrain00006631 From_analysis: Million_mutation_project_reanalysis
      WBStrain00006640 From_analysis: Million_mutation_project_reanalysis
      WBStrain00006643 From_analysis: Million_mutation_project_reanalysis
      WBStrain00006645 From_analysis: Million_mutation_project_reanalysis
      WBStrain00022878 From_analysis: Million_mutation_project_reanalysis
      WBStrain00023138 From_analysis: Million_mutation_project_reanalysis
      WBStrain00024204 From_analysis: Million_mutation_project_reanalysis
      WBStrain00027647 From_analysis: Million_mutation_project_reanalysis
    Laboratory: VC
    Analysis: Million_mutation_project_reanalysis
    Status: Live
  Affects: Gene: WBGene00012005
    Transcript: T24H10.7g.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: T24H10.7g.1:c.275+2300T>C
        Intron_number: 2/3
      T24H10.7f.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: T24H10.7f.1:c.551+2300T>C
        Intron_number: 6/8
      T24H10.7i.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: T24H10.7i.1:c.398+2300T>C
        Intron_number: 3/4
      T24H10.7h.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: T24H10.7h.1:c.509+2300T>C
        Intron_number: 4/5
      T24H10.7a.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: T24H10.7a.1:c.707+2300T>C
        Intron_number: 7/9
      T24H10.7b.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: T24H10.7b.1:c.647+2300T>C
        Intron_number: 7/9
  Method: WGS_Flibotte