WormBase Tree Display for Variation: WBVar00144905

WBVar00144905 Evidence: Paper_evidence: WBPaper00003886
  Name: Public_name: e2663
    Other_name: Y41C4A.14.2:c.256-1G>A
      Y41C4A.14.1:c.256-1G>A
    HGVSg: CHROMOSOME_III:g.11747433G>A
  Sequence_details: SMap: S_parent: Sequence: Y41C4A
    Flanking_sequences: aaaaaagtggcaaaaaacaaaaaaattcca gaattcctgagcatttcggaaaactcgtcg
    Mapping_target: Y41C4A
    Type_of_mutation: Substitution: g a Paper_evidence: WBPaper00003886
    SeqStatus: Sequenced
  Variation_type: Allele
  Origin (4)
  Affects: Gene: WBGene00003417
    Transcript: Y41C4A.14.2 VEP_consequence: splice_acceptor_variant
        VEP_impact: HIGH
        HGVSc: Y41C4A.14.2:c.256-1G>A
        Intron_number: 3/8
      Y41C4A.14.1 VEP_consequence: splice_acceptor_variant
        VEP_impact: HIGH
        HGVSc: Y41C4A.14.1:c.256-1G>A
        Intron_number: 4/9
    Interactor: WBInteraction000008923
      WBInteraction000051783
      WBInteraction000051785
      WBInteraction000501814
      WBInteraction000520835
      WBInteraction000521796
  Genetics: Interpolated_map_position: III 12.0719
    Mapping_data: In_multi_point: 4497
  Description (2)
  Reference (13)
  Method: Substitution_allele