WormBase Tree Display for Variation: WBVar01387451

WBVar01387451 Evidence: Paper_evidence: WBPaper00037807
  Name: Public_name: WBVar01387451
    Other_name: cewivar00190523
      W05G11.6.1:c.1738-33T>C
    HGVSg: CHROMOSOME_III:g.63240A>G
  Sequence_details: SMap: S_parent: Sequence: W05G11
    Flanking_sequences: TCCGATCGCGGTCTCGATCTGGATATTTTTGATGGTTTTGGAAGGTTTTG AGTGGAAAAAACTGAATTTTCTAGTAATTTTCAAGTAAAAGCCTCCAGTT
    Mapping_target: W05G11
    Type_of_mutation: Substitution: a G Paper_evidence: WBPaper00037807
    SeqStatus: Sequenced
  Variation_type: SNP
    Natural_variant
  Origin: Species: Caenorhabditis elegans
    Strain: WBStrain00004602 From_analysis: Million_mutation_project_reanalysis
          WGS_De_Bono
      WBStrain00023191 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 539062902
    Status: Live
  Affects: Gene: WBGene00021043
    Transcript: W05G11.6.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: W05G11.6.1:c.1738-33T>C
        Intron_number: 5/6
  Reference: WBPaper00037807
  Method: WGS_De_Bono