WormBase Tree Display for Variation: WBVar00090290

WBVar00090290 Evidence: Paper_evidence: WBPaper00003698
  Name: Public_name: n1895
    Other_name: F43G9.14:n.56C>T
      F43G9.19:n.50G>A
    HGVSg: CHROMOSOME_I:g.8633348G>A
  Sequence_details: SMap: S_parent: Sequence: F43G9
    Flanking_sequences: tagaaaatagacagacggcgttgaaattag tatgatgtaacaggtcatgaactgtgtcac
    Mapping_target: F43G9
    Type_of_mutation: Substitution: g a Paper_evidence: WBPaper00003698
    SeqStatus: Sequenced
  Variation_type: Allele
  Origin: Species: Caenorhabditis elegans
    Laboratory: MT
    Status: Live
  Affects: Gene: WBGene00195590
      WBGene00201162
    Transcript: F43G9.19 VEP_consequence: non_coding_transcript_exon_variant
        VEP_impact: MODIFIER
        HGVSc: F43G9.19:n.50G>A
        cDNA_position: 50
        Exon_number: 1/1
      F43G9.14 VEP_consequence: non_coding_transcript_exon_variant
        VEP_impact: MODIFIER
        HGVSc: F43G9.14:n.56C>T
        cDNA_position: 56
        Exon_number: 1/1
  Isolation: Mutagen: EMS
  Genetics: Interpolated_map_position: I 3.01058
    Mapping_data: In_multi_point: 1745
        1748
  Reference: WBPaper00015203
  Remark: Manually curated Gene associations preserved as a text remark so that VEP is the canonical predictor of consequence: WBGene00000468 Genomic_neighbourhood
  Method: Substitution_allele