WormBase Tree Display for Variation: WBVar00142950

WBVar00142950 Evidence: Paper_evidence: WBPaper00005417
  Name: Public_name: e78
    Other_name: F41C6.1.2:c.1229G>A
      CE04538:p.Cys410Tyr
      F41C6.1.1:c.1229G>A
    HGVSg: CHROMOSOME_X:g.6894828G>A
  Sequence_details: SMap: S_parent: Sequence: F41C6
    Flanking_sequences: tccatactaaattcaaaaccacttaagctt tggatgtcatccagtcggatcacttggaaa
    Mapping_target: F41C6
    Type_of_mutation: Substitution: g a Paper_evidence: WBPaper00005417
    SeqStatus: Sequenced
  Variation_type: Allele
  Origin: Species: Caenorhabditis elegans
    Strain (12)
    Laboratory: CB
    Status: Live
  Affects: Gene: WBGene00006746
    Transcript: F41C6.1.1 (12)
      F41C6.1.2 (12)
    Interactor: WBInteraction000500108
      WBInteraction000500177
      WBInteraction000500190
      WBInteraction000500384
      WBInteraction000500890
      WBInteraction000500928
      WBInteraction000502341
      WBInteraction000502343
      WBInteraction000556211
  Genetics: Interpolated_map_position: X -2.07168
    Mapping_data: In_2_point: 150
        165
        185
        188
        236
        237
        3385
      In_multi_point (37)
      In_pos_neg_data (16)
  Description: Phenotype (14)
    Phenotype_not_observed: WBPhenotype:0000032 Person_evidence: WBPerson261
        Curator_confirmed: WBPerson712
        Remark: healthy Person_evidence: WBPerson261
            Curator_confirmed: WBPerson712
      WBPhenotype:0000436 Paper_evidence: WBPaper00040857
        Curator_confirmed: WBPerson712
        Remark: Mutation did not cause SNB-1::VENUS localization defects. Paper_evidence: WBPaper00040857
            Curator_confirmed: WBPerson712
      WBPhenotype:0000679 Paper_evidence: WBPaper00035146
        Curator_confirmed: WBPerson712
        Remark: UNC-40::GFP is more ventrally localized as in wild type animals. Paper_evidence: WBPaper00035146
            Curator_confirmed: WBPerson712
      WBPhenotype:0001426 Paper_evidence: WBPaper00004883
        Curator_confirmed: WBPerson712
        Phenotype_assay: Genotype: arIs37 Paper_evidence: WBPaper00004883
              Curator_confirmed: WBPerson712
  Reference (21)
  Method: Substitution_allele