WormBase Tree Display for Variation: WBVar00602647

WBVar00602647 Name: Public_name: WBVar00602647
    Other_name: oicr_ce1066
      oicr_ce1067
      cewivar00330808
      CE23442:p.Pro693Ser
      ZC155.3.1:c.2077C>T
    HGVSg: CHROMOSOME_III:g.5204545G>A
  Sequence_details: SMap: S_parent: Sequence: ZC155
    Flanking_sequences: CTGAGTCATCATCTGATTGATCTCTTCTATTTCTTCTCGAAACTCTTTCAATTGGTCTTTTAGCACGTTGGCGCG TGCTCTGATCGTCAGTGCCTCTTGCGACTCATCCGATTCTTCTCCCATAATCATATCCAATTGTGAACTTGGCGC
    Mapping_target: ZC155
    Type_of_mutation: Substitution: g a
    SeqStatus: Sequenced
  Variation_type: SNP
    Natural_variant
  Origin: Species: Caenorhabditis elegans
    Strain: WBStrain00006629 From_analysis: WGS_Stein
          Million_mutation_project_reanalysis
      WBStrain00006637 From_analysis: Million_mutation_project_reanalysis
      WBStrain00023018 From_analysis: Million_mutation_project_reanalysis
      WBStrain00023072 From_analysis: Million_mutation_project_reanalysis
      WBStrain00023191 From_analysis: Million_mutation_project_reanalysis
      WBStrain00024204 From_analysis: Million_mutation_project_reanalysis
      WBStrain00027649 From_analysis: WGS_Stein
    Analysis: WGS_Stein
      Million_mutation_project_reanalysis
    DB_info: Database: dbSNP_ss ss ss477719532
    History: Acquires_merge: WBVar00602648
    Status: Live
  Affects: Gene: WBGene00022531
    Transcript: ZC155.3.1 VEP_consequence: missense_variant
        VEP_impact: MODERATE
        HGVSc: ZC155.3.1:c.2077C>T
        HGVSp: CE23442:p.Pro693Ser
        cDNA_position: 2094
        CDS_position: 2077
        Protein_position: 693
        Exon_number: 7/10
        Codon_change: Ccg/Tcg
        Amino_acid_change: P/S
  Remark: validatation rate is over 97%
  Method: WGS_Stein