WormBase Tree Display for Variation: WBVar01468139

WBVar01468139 Evidence: Paper_evidence: WBPaper00040707
  Name: Public_name: WBVar01468139
    Other_name: cewivar00561725
      M02F4.1.1:c.850-31C>G
    HGVSg: CHROMOSOME_X:g.3027525G>C
  Sequence_details: SMap: S_parent: Sequence: M02F4
    Flanking_sequences: CTGAAAATTCGTAATGCCAAATAAGGTAAA ATTTCGAGCAAACGCAAATTTCGAACAAAC
    Mapping_target: M02F4
    Type_of_mutation: Substitution: g c
    SeqStatus: Sequenced
  Variation_type: SNP
    Natural_variant
  Origin: Species: Caenorhabditis elegans
    Strain: WBStrain00005309 From_analysis: WGS_Andersen
      WBStrain00006697 From_analysis: WGS_Andersen
      WBStrain00006698 From_analysis: WGS_Andersen
      WBStrain00023018 From_analysis: Million_mutation_project_reanalysis
          WGS_Andersen
      WBStrain00024204 From_analysis: Million_mutation_project_reanalysis
          WGS_Andersen
      WBStrain00040481 From_analysis: WGS_Andersen
      WBStrain00040482 From_analysis: WGS_Andersen
    Laboratory: QX
    Person: WBPerson1730
    Analysis: Million_mutation_project_reanalysis
      WGS_Andersen
    DB_info: Database: dbSNP_rs rs 193353441
        dbSNP_ss ss 295529360
    Status: Live
  Affects: Gene: WBGene00019735
    Transcript: M02F4.1.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: M02F4.1.1:c.850-31C>G
        Intron_number: 5/7
  Reference: WBPaper00040707
  Method: WGS_Andersen