WormBase Tree Display for Variation: WBVar00225729

WBVar00225729 Evidence: Paper_evidence: WBPaper00037807
  Name: Public_name: WBVar00225729
    Other_name: pas37505
      cewivar00091310
      C52E12.2b.1:c.1470-147C>T
      C52E12.2a.2:c.1470-147C>T
      C52E12.2a.1:c.1470-147C>T
    HGVSg: CHROMOSOME_II:g.7003247C>T
  Sequence_details: SMap: S_parent: Sequence: C52E12
    Flanking_sequences: TCTCCAACCCAAATATGAACGCGGCGCCTATCTATGCTTCAAAAAGTCTT GTTAGAAAGACTGAATAAAACATGCGGGGGTATAGCTCAGTGGTAGAGCG
    Mapping_target: C52E12
    Type_of_mutation: Substitution: C T
    SeqStatus: Sequenced
  Variation_type: SNP
    Predicted_SNP
    Natural_variant
  Origin: Species: Caenorhabditis elegans
    Strain (37)
    Laboratory: AX
    Person: WBPerson6900
    Analysis: WGS_Pasadena_Quinlan
      WGS_De_Bono
      Million_mutation_project_reanalysis
    History: Acquires_merge: WBVar01373014
        WBVar01240975
        WBVar01307353
    Status: Live
  Affects: Gene: WBGene00006831
    Transcript: C52E12.2a.2 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: C52E12.2a.2:c.1470-147C>T
        Intron_number: 8/23
      C52E12.2b.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: C52E12.2b.1:c.1470-147C>T
        Intron_number: 8/24
      C52E12.2a.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: C52E12.2a.1:c.1470-147C>T
        Intron_number: 8/23
  Reference: WBPaper00037807
  Method: WGS_Pasadena_Quinlan