WormBase Tree Display for Variation: WBVar01747523

WBVar01747523 Name: Public_name: WBVar01747523
    Other_name: cewivar00446927
      T20B3.7.2:c.208+355G>A
      T20B3.7.1:c.208+355G>A
      T20B3.2.1:c.691C>T
      CE20087:p.Pro231Ser
    HGVSg: CHROMOSOME_V:g.16833878G>A
  Sequence_details: SMap: S_parent: Sequence: T20B3
    Flanking_sequences: CGGCGGCTTCTGGTTCTGGCTCGGCCTCTG CTCGACTGGAGCAGCTAGTTCCACTGGTGC
    Mapping_target: T20B3
    Source_location: 225 CHROMOSOME_V 16833856 16833856 From_analysis: Million_mutation_project_reanalysis
    Type_of_mutation: Substitution: G A
    SeqStatus: Sequenced
  Variation_type: Natural_variant
  Origin: Species: Caenorhabditis elegans
    Strain: WBStrain00023139 From_analysis: Million_mutation_project_reanalysis
      WBStrain00027648 From_analysis: Million_mutation_project_reanalysis
      WBStrain00027660 From_analysis: Million_mutation_project_reanalysis
      WBStrain00027662 From_analysis: Million_mutation_project_reanalysis
    Laboratory: VC
    Analysis: Million_mutation_project_reanalysis
    Status: Live
  Affects: Gene: WBGene00006585
      WBGene00004026
    Transcript: T20B3.2.1 VEP_consequence: missense_variant
        VEP_impact: MODERATE
        HGVSc: T20B3.2.1:c.691C>T
        HGVSp: CE20087:p.Pro231Ser
        cDNA_position: 710
        CDS_position: 691
        Protein_position: 231
        Exon_number: 5/6
        Codon_change: Cca/Tca
        Amino_acid_change: P/S
      T20B3.7.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: T20B3.7.1:c.208+355G>A
        Intron_number: 3/7
      T20B3.7.2 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: T20B3.7.2:c.208+355G>A
        Intron_number: 2/6
  Method: WGS_Flibotte