WormBase Tree Display for Variation: WBVar01553250

WBVar01553250 Name: Public_name: WBVar01553250
    Other_name: cewivar00130541
      Y15E3A.1a.1:c.1319+120T>C
      Y15E3A.1b.2:c.827+120T>C
      Y15E3A.1a.4:c.1319+120T>C
      Y15E3A.1a.3:c.1319+120T>C
      Y15E3A.1a.2:c.1319+120T>C
      Y15E3A.1b.1:c.827+120T>C
    HGVSg: CHROMOSOME_X:g.15314188T>C
  Sequence_details: SMap: S_parent: Sequence: Y15E3A
    Flanking_sequences: ATTTTTAATTGCTTATTCATATCCGTAAAA TTGCTAAGTTGGCAAAAGTGAATAGTTTTC
    Mapping_target: Y15E3A
    Source_location: 225 CHROMOSOME_X 15314119 15314119 From_analysis: Million_mutation_project_reanalysis
    Type_of_mutation: Substitution: T C
    SeqStatus: Sequenced
  Variation_type: Natural_variant
  Origin: Species: Caenorhabditis elegans
    Strain: WBStrain00004599 From_analysis: Million_mutation_project_reanalysis
      WBStrain00006631 From_analysis: Million_mutation_project_reanalysis
      WBStrain00006643 From_analysis: Million_mutation_project_reanalysis
      WBStrain00006645 From_analysis: Million_mutation_project_reanalysis
      WBStrain00008273 From_analysis: Million_mutation_project_reanalysis
      WBStrain00023138 From_analysis: Million_mutation_project_reanalysis
    Laboratory: VC
    Analysis: Million_mutation_project_reanalysis
    Status: Live
  Affects: Gene: WBGene00003681
    Transcript: Y15E3A.1a.4 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: Y15E3A.1a.4:c.1319+120T>C
        Intron_number: 9/10
      Y15E3A.1b.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: Y15E3A.1b.1:c.827+120T>C
        Intron_number: 6/7
      Y15E3A.1a.2 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: Y15E3A.1a.2:c.1319+120T>C
        Intron_number: 9/10
      Y15E3A.1b.2 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: Y15E3A.1b.2:c.827+120T>C
        Intron_number: 8/9
      Y15E3A.1a.3 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: Y15E3A.1a.3:c.1319+120T>C
        Intron_number: 9/10
      Y15E3A.1a.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: Y15E3A.1a.1:c.1319+120T>C
        Intron_number: 9/10
  Method: WGS_Flibotte