WormBase Tree Display for Variation: WBVar01468111

WBVar01468111 Evidence: Paper_evidence: WBPaper00040707
  Name: Public_name: WBVar01468111
    Other_name: cewivar00525160
      CE35802:p.Asp243=
      Y41G9A.3.1:c.729T>C
    HGVSg: CHROMOSOME_X:g.2979074T>C
  Sequence_details: SMap: S_parent: Sequence: Y41G9A
    Flanking_sequences: ACTTCCCGTCATGGATGAGAAGACGGGAGA TGTGCGTACATATTGACACATCGTAGGATA
    Mapping_target: Y41G9A
    Type_of_mutation: Substitution: t c
    SeqStatus: Sequenced
  Variation_type: SNP
    Natural_variant
  Origin: Species: Caenorhabditis elegans
    Strain: WBStrain00022850 From_analysis: Million_mutation_project_reanalysis
          WGS_Andersen
      WBStrain00023072 From_analysis: Million_mutation_project_reanalysis
          WGS_Andersen
      WBStrain00023079 From_analysis: WGS_Andersen
      WBStrain00023084 From_analysis: WGS_Andersen
    Laboratory: QX
    Person: WBPerson1730
    Analysis: Million_mutation_project_reanalysis
      WGS_Andersen
    DB_info: Database: dbSNP_rs rs 193353413
        dbSNP_ss ss 295529332
    Status: Live
  Affects: Gene: WBGene00021527
    Transcript: Y41G9A.3.1 VEP_consequence: synonymous_variant
        VEP_impact: LOW
        HGVSc: Y41G9A.3.1:c.729T>C
        HGVSp: CE35802:p.Asp243=
        cDNA_position: 754
        CDS_position: 729
        Protein_position: 243
        Exon_number: 8/14
        Codon_change: gaT/gaC
        Amino_acid_change: D
  Reference: WBPaper00040707
  Method: WGS_Andersen