WormBase Tree Display for Variation: WBVar00089629

WBVar00089629 Evidence: Paper_evidence: WBPaper00000486
      WBPaper00006135
  Name: Public_name: n619
    Other_name: R09G11.1.1:c.262G>A
      CE12656:p.Glu88Lys
    HGVSg: CHROMOSOME_X:g.17530208G>A
  Sequence_details: SMap: S_parent: Sequence: R09G11
    Flanking_sequences: ttcaatcagaagaaaggatatcaagagccc agacaattacttattactatcacacttacc
    Mapping_target: R09G11
    Type_of_mutation: Substitution: g a Paper_evidence: WBPaper00000486
              WBPaper00006135
    SeqStatus: Sequenced
  Variation_type: Allele
  Origin: Species: Caenorhabditis elegans
    Laboratory: MT
    Status: Live
  Affects: Gene: WBGene00006319
    Transcript: R09G11.1.1 VEP_consequence: missense_variant
        VEP_impact: MODERATE
        SIFT: 0.05 deleterious
        PolyPhen: 0.944 possibly_damaging
        HGVSc: R09G11.1.1:c.262G>A
        HGVSp: CE12656:p.Glu88Lys
        cDNA_position: 328
        CDS_position: 262
        Protein_position: 88
        Exon_number: 4/8
        Codon_change: Gag/Aag
        Amino_acid_change: E/K
  Isolation: Mutagen: EMS
  Genetics: Interpolated_map_position: X 24.1669
  Reference: WBPaper00000486
    WBPaper00006135
  Remark: Greenwald and Horvitz (1980)
  Method: Substitution_allele