WormBase Tree Display for Variation: WBVar00090789

WBVar00090789 Evidence: Paper_evidence: WBPaper00031335
  Name: Public_name: n4099
    Other_name: CE29914:p.Ser2239IlefsTer18
      Y71G12B.11d.1:c.3589_4285del
      Y71G12B.11b.1:c.*4020_*4716del
      Y71G12B.11e.1:c.5620_6316del
      Y71G12B.11a.1:c.6715_7411del
      CE50474:p.Ser1874IlefsTer18
      CE46470:p.Ser1576IlefsTer18
      Y71G12B.11c.1:c.4726_5422del
      CE49571:p.Ser1197IlefsTer18
    HGVSg: CHROMOSOME_I:g.1738180_1739175del
  Sequence_details: SMap: S_parent: Sequence: Y71G12B
    Flanking_sequences: GCCGTGAGGTCCCTGCTCGCCGTGGTGCGAACCATC ATCGGAGATTGCAGGCTG
    Mapping_target: Y71G12B
    Type_of_mutation: Deletion
    SeqStatus: Sequenced
  Variation_type: Allele
  Origin: Species: Caenorhabditis elegans
    Laboratory: MT
    Status: Live
  Affects: Gene: WBGene00006771
      WBGene00003278
      WBGene00199017
    Transcript: Y71G12B.36 VEP_consequence: transcript_ablation
        VEP_impact: HIGH
        Exon_number: 1/1
      Y71G12B.11c.1 (11)
      Y71G12B.29
      Y71G12B.11e.1 (11)
      Y71G12B.11a.1 (11)
      Y71G12B.11d.1 (11)
      Y71G12B.11b.1 VEP_consequence: splice_acceptor_variant,splice_donor_variant,3_prime_UTR_variant,intron_variant
        VEP_impact: HIGH
        HGVSc: Y71G12B.11b.1:c.*4020_*4716del
        cDNA_position: 7018-7714
        Intron_number: 11/12
        Exon_number: 11-12/13
  Isolation: Mutagen: UV-TMP Paper_evidence: WBPaper00031335
  Genetics: Interpolated_map_position: I -13.1255
  Description: Phenotype: WBPhenotype:0000062 Paper_evidence: WBPaper00031335
        Curator_confirmed: WBPerson2021
        Variation_effect: Probable_null_via_phenotype: Paper_evidence: WBPaper00031335
            Curator_confirmed: WBPerson2021
  Reference: WBPaper00031335
  Method: Deletion_allele