WormBase Tree Display for Variation: WBVar00054417

WBVar00054417 Name: Public_name: ct46
    Other_name: T01G9.5a.1:c.296C>T
      CE06342:p.Pro99Leu
      CE32479:p.Pro99Leu
      T01G9.5b.1:c.296C>T
    HGVSg: CHROMOSOME_I:g.8295227C>T
  Sequence_details: SMap: S_parent: Sequence: T01G9
    Flanking_sequences: aaagtggaagtccagagccacctgcagacc agatgtttggtccaaaccatcgccaccgtt
    Mapping_target: T01G9
    Type_of_mutation: Substitution: c t Person_evidence: WBPerson399
    SeqStatus: Sequenced
  Variation_type: Allele
  Origin: Species: Caenorhabditis elegans
    Strain: WBStrain00008444
      WBStrain00026463
    Laboratory: BW
    Status: Live
  Linked_to: WBVar00054422
    WBVar00054427
    WBVar02125078
  Affects: Gene: WBGene00003183
    Transcript: T01G9.5a.1 (12)
      T01G9.5b.1 VEP_consequence: missense_variant
        VEP_impact: MODERATE
        SIFT: 0 deleterious
        PolyPhen: 0.997 probably_damaging
        HGVSc: T01G9.5b.1:c.296C>T
        HGVSp: CE32479:p.Pro99Leu
        cDNA_position: 304
        CDS_position: 296
        Protein_position: 99
        Exon_number: 3/6
        Codon_change: cCa/cTa
        Amino_acid_change: P/L
    Interactor: WBInteraction000051975
      WBInteraction000051979
      WBInteraction000051980
      WBInteraction000051982
      WBInteraction000519223
      WBInteraction000519224
      WBInteraction000556055
      WBInteraction000556056
      WBInteraction000578852
  Isolation: Mutagen: EMS
  Genetics: Interpolated_map_position: I 2.70613
    Mapping_data: In_multi_point: 1764
        1765
  Description: Phenotype (6)
  Reference (12)
  Method: Substitution_allele