WormBase Tree Display for Variation: WBVar01444113

WBVar01444113 Evidence: Paper_evidence: WBPaper00040707
  Name: Public_name: WBVar01444113
    Other_name: cewivar00549591
      M01E10.2a.1:c.3654+34C>G
      M01E10.2b.1:c.2655+34C>G
    HGVSg: CHROMOSOME_III:g.2037846G>C
  Sequence_details: SMap: S_parent: Sequence: M01E10
    Flanking_sequences: TGGAATTCAATTTTTTACTTAGTTTGCTTT AAAATTGCGGGAAATTGCTGCAAGCGGGCT
    Mapping_target: M01E10
    Type_of_mutation: Substitution: g c
    SeqStatus: Sequenced
  Variation_type: SNP
    Natural_variant
  Origin: Species: Caenorhabditis elegans
    Strain: WBStrain00022928 From_analysis: WGS_Andersen
      WBStrain00022930 From_analysis: Million_mutation_project_reanalysis
          WGS_Andersen
      WBStrain00023150 From_analysis: WGS_Andersen
      WBStrain00023211 From_analysis: WGS_Andersen
    Laboratory: QX
    Person: WBPerson1730
    Analysis: Million_mutation_project_reanalysis
      WGS_Andersen
    DB_info: Database: dbSNP_rs rs 193331274
        dbSNP_ss ss 295507193
    Status: Live
  Affects: Gene: WBGene00001063
    Transcript: M01E10.2a.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: M01E10.2a.1:c.3654+34C>G
        Intron_number: 15/21
      M01E10.2b.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: M01E10.2b.1:c.2655+34C>G
        Intron_number: 10/16
  Reference: WBPaper00040707
  Method: WGS_Andersen