WormBase Tree Display for Variation: WBVar01441334

WBVar01441334 Evidence: Paper_evidence: WBPaper00040707
  Name: Public_name: WBVar01441334
    Other_name: F29C12.5.1:c.961-26C>T
    HGVSg: CHROMOSOME_II:g.13124224C>T
  Sequence_details: SMap: S_parent: Sequence: F29C12
    Flanking_sequences: CAGGTGTGTTTTTCTTTCCTATTGTAATTT ATATTGTAATTTCATATTTTTCCAGATCCT
    Mapping_target: F29C12
    Type_of_mutation: Substitution: c t
    SeqStatus: Sequenced
  Variation_type: SNP
    Natural_variant
  Origin: Species: Caenorhabditis elegans
    Strain (135)
    Laboratory: QX
    Person: WBPerson1730
    Analysis: WGS_Andersen
    DB_info: Database: dbSNP_rs rs 193328920
        dbSNP_ss ss 295504839
    Status: Live
  Affects: Gene: WBGene00009247
    Transcript: F29C12.5.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: F29C12.5.1:c.961-26C>T
        Intron_number: 6/9
  Reference: WBPaper00040707
  Method: WGS_Andersen