WormBase Tree Display for Variation: WBVar01258672

WBVar01258672 Evidence: Paper_evidence: WBPaper00037807
  Name: Public_name: WBVar01258672
    Other_name: cewivar00285127
      M01E10.2a.1:c.2352+82A>G
      M01E10.2b.1:c.1353+475A>G
    HGVSg: CHROMOSOME_III:g.2041554T>C
  Sequence_details: SMap: S_parent: Sequence: M01E10
    Flanking_sequences: TGTGTAGATTTACGGCGGTCCTACGTAGATTTACGGGAGGTCTATGTGGA TTACGGGGATCTGTGTAGACTTCCAAAACACTATGCAGATTTACGGGCTG
    Mapping_target: M01E10
    Type_of_mutation: Substitution: t C Paper_evidence: WBPaper00037807
    SeqStatus: Sequenced
  Variation_type: SNP
    Natural_variant
  Origin: Species: Caenorhabditis elegans
    Strain: WBStrain00006622 From_analysis: Million_mutation_project_reanalysis
      WBStrain00006642 From_analysis: WGS_De_Bono
      WBStrain00006643 From_analysis: Million_mutation_project_reanalysis
      WBStrain00006645 From_analysis: Million_mutation_project_reanalysis
      WBStrain00022852 From_analysis: Million_mutation_project_reanalysis
      WBStrain00022856 From_analysis: Million_mutation_project_reanalysis
      WBStrain00022878 From_analysis: Million_mutation_project_reanalysis
      WBStrain00027647 From_analysis: Million_mutation_project_reanalysis
    Laboratory: AX
    Analysis: WGS_De_Bono
      Million_mutation_project_reanalysis
    DB_info: Database: dbSNP_ss ss 539094749
    Status: Live
  Affects: Gene: WBGene00001063
    Transcript: M01E10.2a.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: M01E10.2a.1:c.2352+82A>G
        Intron_number: 11/21
      M01E10.2b.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: M01E10.2b.1:c.1353+475A>G
        Intron_number: 6/16
  Reference: WBPaper00037807
  Method: WGS_De_Bono