WormBase Tree Display for Variation: WBVar01242917

WBVar01242917 Evidence: Paper_evidence: WBPaper00037807
  Name: Public_name: WBVar01242917
    Other_name: cewivar00139905
      T24H10.7a.1:c.184+1544T>C
      T24H10.7f.1:c.-113T>C
      T24H10.7b.1:c.124+1544T>C
    HGVSg: CHROMOSOME_II:g.9118440T>C
  Sequence_details: SMap: S_parent: Sequence: T24H10
    Flanking_sequences: GTGAGCTGTCTCGTTGAGCTGCTCTGAGAAATCGAGAGAGAGAGCCCTTG CCACTACTTGCTCATTGAGCACAGAACGCAGAATTCTTGAGTTCTGGATT
    Mapping_target: T24H10
    Type_of_mutation: Substitution: t C Paper_evidence: WBPaper00037807
    SeqStatus: Sequenced
  Variation_type: SNP
    Natural_variant
  Origin: Species: Caenorhabditis elegans
    Strain (22)
    Laboratory: AX
      QX
    Person: WBPerson1730
    Analysis: WGS_De_Bono
      Million_mutation_project_reanalysis
      WGS_Andersen
    DB_info: Database: dbSNP_ss ss 539080569
    History: Acquires_merge: WBVar01438983
    Status: Live
  Affects: Gene: WBGene00012005
    Transcript: T24H10.7f.1 VEP_consequence: 5_prime_UTR_variant
        VEP_impact: MODIFIER
        HGVSc: T24H10.7f.1:c.-113T>C
        cDNA_position: 18
        Exon_number: 1/9
      T24H10.7a.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: T24H10.7a.1:c.184+1544T>C
        Intron_number: 3/9
      T24H10.7b.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: T24H10.7b.1:c.124+1544T>C
        Intron_number: 3/9
  Reference: WBPaper00040707
    WBPaper00037807
  Method: WGS_De_Bono