WormBase Tree Display for Variation: WBVar00089583

WBVar00089583 Evidence: Paper_evidence: WBPaper00004497
  Name: Public_name: n531
    Other_name: T25C12.1a.1:c.873+1G>A
      T25C12.1b.1:c.867+1G>A
    HGVSg: CHROMOSOME_X:g.11483283G>A
  Sequence_details: SMap: S_parent: Sequence: T25C12
    Flanking_sequences: aaggctggtggtccagaacgaaaaccaagg tttgtataaagtattaaatttcacaagtca
    Mapping_target: T25C12
    Type_of_mutation: Substitution: g a Paper_evidence: WBPaper00004497
    SeqStatus: Sequenced
  Variation_type: Allele
  Origin: Species: Caenorhabditis elegans
    Laboratory: MT
    Status: Live
  Affects: Gene: WBGene00003003
    Transcript: T25C12.1b.1 VEP_consequence: splice_donor_variant
        VEP_impact: HIGH
        HGVSc: T25C12.1b.1:c.867+1G>A
        Intron_number: 6/11
      T25C12.1a.1 VEP_consequence: splice_donor_variant
        VEP_impact: HIGH
        HGVSc: T25C12.1a.1:c.873+1G>A
        Intron_number: 8/13
  Isolation: Mutagen: EMS Paper_evidence: WBPaper00004497
  Genetics: Interpolated_map_position: X 3.8622
  Reference: WBPaper00004497
  Remark: This substitution affects both isoforms Paper_evidence: WBPaper00004497
  Method: Substitution_allele