WormBase Tree Display for Variation: WBVar00143951

WBVar00143951 Evidence: Paper_evidence: WBPaper00004623
  Name: Public_name: e1372
    Other_name: B0412.2.1:c.369+1G>A
    HGVSg: CHROMOSOME_III:g.812434G>A
  Sequence_details: SMap: S_parent: Sequence: B0412
    Flanking_sequences: aatgatttggaaagaagcgatattcttcag tatcgtttggtttttttttaaaaagaatcc
    Mapping_target: B0412
    Type_of_mutation: Substitution: g a Paper_evidence: WBPaper00004623
    SeqStatus: Sequenced
  Variation_type: Allele
  Origin: Species: Caenorhabditis elegans
    Strain: WBStrain00000063
      WBStrain00004310
      WBStrain00005597
      WBStrain00006202
      WBStrain00006360
      WBStrain00022755
      WBStrain00023548
      WBStrain00026329
      WBStrain00026330
      WBStrain00026331
      WBStrain00035147
      WBStrain00035150
      WBStrain00050822
      WBStrain00050823
      WBStrain00050824
      WBStrain00050825
      WBStrain00050852
      WBStrain00051573
    Laboratory: CB
    Status: Live
  Affects: Gene: WBGene00000903
    Transcript: B0412.2.1 VEP_consequence: splice_donor_variant
        VEP_impact: HIGH
        HGVSc: B0412.2.1:c.369+1G>A
        Intron_number: 3/6
    Interactor (86)
  Isolation: Mutagen: EMS Paper_evidence: WBPaper00004623
  Genetics: Interpolated_map_position: III -25.7993
    Mapping_data: In_2_point: 273
        422
        423
        2720
        2721
        4974
        6130
      In_multi_point (25)
      In_pos_neg_data: 1585
        1592
  Description: Phenotype (34)
    Phenotype_not_observed (15)
  Reference (65)
  Method: Substitution_allele