WormBase Tree Display for Variation: WBVar00274919

WBVar00274919 Evidence: Paper_evidence: WBPaper00035146
  Name: Public_name: ur282
    Other_name: F41C6.1.2:c.646C>T
      CE04538:p.Pro216Ser
      F41C6.1.1:c.646C>T
    HGVSg: CHROMOSOME_X:g.6890885C>T
  Sequence_details: SMap: S_parent: Sequence: F41C6
    Flanking_sequences: taatgggtccaggaggaaaccgtgtagcgttc cttttctagagaacagaccttctgcacaaaa
    Mapping_target: F41C6
    Type_of_mutation: Substitution: c t Paper_evidence: WBPaper00035146
    SeqStatus: Sequenced
  Variation_type: Allele
  Origin: Species: Caenorhabditis elegans
    Strain: WBStrain00022117
      WBStrain00022118
      WBStrain00022119
      WBStrain00022125
      WBStrain00022137
      WBStrain00022138
      WBStrain00022146
      WBStrain00022147
    Laboratory: IM
    Status: Live
  Affects: Gene: WBGene00006746
    Transcript: F41C6.1.1 VEP_consequence: missense_variant
        VEP_impact: MODERATE
        HGVSc: F41C6.1.1:c.646C>T
        HGVSp: CE04538:p.Pro216Ser
        cDNA_position: 712
        CDS_position: 646
        Protein_position: 216
        Exon_number: 4/15
        Codon_change: Cct/Tct
        Amino_acid_change: P/S
      F41C6.1.2 VEP_consequence: missense_variant
        VEP_impact: MODERATE
        HGVSc: F41C6.1.2:c.646C>T
        HGVSp: CE04538:p.Pro216Ser
        cDNA_position: 712
        CDS_position: 646
        Protein_position: 216
        Exon_number: 4/16
        Codon_change: Cct/Tct
        Amino_acid_change: P/S
    Interactor: WBInteraction000500102
      WBInteraction000500105
      WBInteraction000500180
      WBInteraction000500185
      WBInteraction000500186
  Genetics: Interpolated_map_position: X -2.09736
  Reference: WBPaper00035146
  Method: Substitution_allele