WormBase Tree Display for Variation: WBVar00241199

WBVar00241199 Evidence: Person_evidence: WBPerson2653
  Name: Public_name: qa704
    Other_name: F22D6.11.1:c.481_753+100del
    HGVSg: CHROMOSOME_I:g.7110944_7111371del
  Sequence_details: SMap: S_parent: Sequence: F22D6
    Flanking_sequences: ggcgaaaattcagctccaatttttcaaaat ttggtaatgtgccagaactgtgactgagaa
    Mapping_target: F22D6
    Type_of_mutation: Deletion
    SeqStatus: Sequenced
  Variation_type: Allele
  Origin: Species: Caenorhabditis elegans
    Strain: WBStrain00040602
    Laboratory: XA
    Status: Live
  Affects: Gene: WBGene00001643
    Transcript: F22D6.11.1 VEP_consequence: splice_acceptor_variant,splice_donor_variant,coding_sequence_variant,intron_variant
        VEP_impact: HIGH
        HGVSc: F22D6.11.1:c.481_753+100del
        cDNA_position: 487-?
        CDS_position: 481-?
        Protein_position: 161-?
        Intron_number: 5-6/9
        Exon_number: 5-6/10
  Isolation: Mutagen: EMS
  Genetics: Interpolated_map_position: I 1.74971
    Mapping_data: In_multi_point: 4364
  Description: Phenotype_not_observed: WBPhenotype:0000517 Paper_evidence: WBPaper00005030
        Curator_confirmed: WBPerson557
      WBPhenotype:0000518 Paper_evidence: WBPaper00005030
        Curator_confirmed: WBPerson557
      WBPhenotype:0000520 Paper_evidence: WBPaper00005030
        Curator_confirmed: WBPerson557
      WBPhenotype:0000604 Paper_evidence: WBPaper00005030
        Curator_confirmed: WBPerson557
      WBPhenotype:0000643 Paper_evidence: WBPaper00005030
        Curator_confirmed: WBPerson557
      WBPhenotype:0000886 Person_evidence: WBPerson2653
        Curator_confirmed: WBPerson712
        Remark: This mutation causes no obvious phenotype. Person_evidence: WBPerson2653
            Curator_confirmed: WBPerson712
  Reference: WBPaper00005030
  Method: Deletion_allele