WormBase Tree Display for Variation: WBVar00087804

WBVar00087804 Evidence: Paper_evidence: WBPaper00001669
      WBPaper00005276
  Name: Public_name: hc143
    Other_name: Y66D12A.20.1:c.581C>T
      CE28799:p.Thr194Ile
    HGVSg: CHROMOSOME_III:g.11508260C>T
  Sequence_details: SMap: S_parent: Sequence: Y66D12A
    Flanking_sequences: cgccgagaaccgctgcagcactgatgggaa ttttcaatattgtgcagtttctgcccactc
    Mapping_target: Y66D12A
    Type_of_mutation: Substitution: c t Paper_evidence: WBPaper00001669
    SeqStatus: Sequenced
  Variation_type: Allele
  Origin: Species: Caenorhabditis elegans
    Laboratory: BA
    Author: Jacob Varkey
      Alicia Minniti
    Status: Live
  Affects: Gene: WBGene00004960
    Transcript: Y66D12A.20.1 (12)
  Isolation: Mutagen: EMS Paper_evidence: WBPaper00001669
  Genetics: Interpolated_map_position: III 10.5695
  Description: Phenotype: WBPhenotype:0000688 Person_evidence: WBPerson438
        Curator_confirmed: WBPerson48
      WBPhenotype:0001498 Person_evidence: WBPerson438
        Curator_confirmed: WBPerson48
        Remark: defective spermatocytes, defective major sperm protein assembly Person_evidence: WBPerson438
            Curator_confirmed: WBPerson48
  Reference: WBPaper00005276
    WBPaper00001669
  Method: Substitution_allele