WormBase Tree Display for Variation: WBVar01429664

WBVar01429664 Evidence: Paper_evidence: WBPaper00040707
  Name: Public_name: WBVar01429664
    Other_name: cewivar00370757
      Y74C9A.4a.1:c.850-1118T>C
      Y74C9A.4b.1:c.859-1118T>C
      Y74C9A.4c.1:c.766-1118T>C
    HGVSg: CHROMOSOME_I:g.22257A>G
  Sequence_details: SMap: S_parent: Sequence: Y74C9A
    Flanking_sequences: AAAATTTAAAAAGTAGAATATAACTGTGAG AAATTTCCAAAATTGTCAAAATTTCAAATA
    Mapping_target: Y74C9A
    Type_of_mutation: Substitution: a g
    SeqStatus: Sequenced
  Variation_type: SNP
    Natural_variant
  Origin: Species: Caenorhabditis elegans
    Strain: WBStrain00006632 From_analysis: WGS_Andersen
      WBStrain00006640 From_analysis: Million_mutation_project_reanalysis
          WGS_Andersen
      WBStrain00023071 From_analysis: WGS_Andersen
      WBStrain00023105 From_analysis: WGS_Andersen
      WBStrain00023106 From_analysis: WGS_Andersen
      WBStrain00027647 From_analysis: Million_mutation_project_reanalysis
          WGS_Andersen
      WBStrain00027653 From_analysis: WGS_Andersen
      WBStrain00027656 From_analysis: WGS_Andersen
    Laboratory: QX
    Person: WBPerson1730
    Analysis: Million_mutation_project_reanalysis
      WGS_Andersen
    DB_info: Database: dbSNP_rs rs 193317727
        dbSNP_ss ss 295493644
    Status: Live
  Affects: Gene: WBGene00022278
    Transcript: Y74C9A.4a.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: Y74C9A.4a.1:c.850-1118T>C
        Intron_number: 7/13
      Y74C9A.4b.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: Y74C9A.4b.1:c.859-1118T>C
        Intron_number: 7/13
      Y74C9A.4c.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: Y74C9A.4c.1:c.766-1118T>C
        Intron_number: 5/10
  Reference: WBPaper00040707
  Method: WGS_Andersen