WormBase Tree Display for Variation: WBVar01462647

WBVar01462647 Evidence: Paper_evidence: WBPaper00040707
  Name: Public_name: WBVar01462647
    Other_name: cewivar00585159
      F35E12.6.1:c.703T>G
      F35E12.6.2:c.703T>G
      CE35523:p.Ser235Ala
    HGVSg: CHROMOSOME_V:g.13734956A>C
  Sequence_details: SMap: S_parent: Sequence: F35E12
    Flanking_sequences: ATATAAATTCTAATGAGAAATAGTTACCTG TGCGTCGTTTGCAAGTAACATTGAATTAGA
    Mapping_target: F35E12
    Type_of_mutation: Substitution: a c
    SeqStatus: Sequenced
  Variation_type: SNP
    Natural_variant
  Origin: Species: Caenorhabditis elegans
    Strain: 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 193348303
        dbSNP_ss ss 295524222
    Status: Live
  Affects: Gene: WBGene00009430
    Transcript: F35E12.6.1 VEP_consequence: missense_variant
        VEP_impact: MODERATE
        HGVSc: F35E12.6.1:c.703T>G
        HGVSp: CE35523:p.Ser235Ala
        cDNA_position: 706
        CDS_position: 703
        Protein_position: 235
        Exon_number: 7/11
        Codon_change: Tca/Gca
        Amino_acid_change: S/A
      F35E12.6.2 VEP_consequence: missense_variant
        VEP_impact: MODERATE
        HGVSc: F35E12.6.2:c.703T>G
        HGVSp: CE35523:p.Ser235Ala
        cDNA_position: 743
        CDS_position: 703
        Protein_position: 235
        Exon_number: 8/12
        Codon_change: Tca/Gca
        Amino_acid_change: S/A
  Reference: WBPaper00040707
  Method: WGS_Andersen